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Tag: Recalls

  • Frozen waffle products recalled due to possible listeria contamination

    Frozen waffle products recalled due to possible listeria contamination

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    OAK BROOK, Ill. — Hundreds of frozen waffle products sold in leading retailers including Publix, Walmart and Target are being recalled because of possible contamination by the listeria bacteria, according to the manufacturer.

    What You Need To Know

    • Hundreds of frozen waffle products sold at Publix, Walmart, Target and other retailers have been recalled due to possible listeria contamination

    • TreeHouse Foods said that it issued a voluntary recall after discovering possible contamination during routing testing at its plant

    • The illness is most dangerous to pregnant women, newborns, adults over 65 and people with weakened immune systems

    TreeHouse Foods said Friday that it issued a voluntary recall after discovering possible contamination during routing testing at its plant. It said the U.S. Food and Drug Administration and Canadian food regulators are aware of the recall.

    Listeria infections can cause mild illness including fever and diarrhea or more serious problems. The illness is most dangerous to pregnant women, newborns, adults over 65 and people with weakened immune systems, according to the U.S. Centers for Disease Control.

    The CDC estimates that 1,600 people are infected with listeria each year in the United States and 260 die.

    The recalled waffles are sold under a variety of names including Walmart’s Great Value, Target’s Good & Gather and private label brands sold by Food Lion, Kroger and Schnucks. TreeHouse published a complete list.

    TreeHouse said there have been no confirmed reports of illness related to the waffles.

    The company said consumers holding any of the products should dispose of them or return them to the store for credit.

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    Spectrum News Staff, Associated Press

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  • 13 DC schools may be affected by nationwide listeria recall of meat and poultry – WTOP News

    13 DC schools may be affected by nationwide listeria recall of meat and poultry – WTOP News

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    Nearly 12 million pounds of potentially contaminated meat is being recalled across the U.S. and some of those contaminated products were sent to schools in the District, the U.S. Department of Agriculture’s (USDA) Food Safety and Inspection Service says.

    Nearly 12 million pounds of potentially contaminated meat is being recalled across the U.S. and some of those contaminated products were sent to schools in the District, the U.S. Department of Agriculture’s (USDA) Food Safety and Inspection Service says.

    A recall of ready-to-eat meat and poultry items made by Oklahoma-based BrucePac was expanded Thursday to include nearly 1.8 million pounds of additional products recalled over possible listeria contamination. The USDA released a list of schools across the U.S. that received the potentially contaminated products, with schools in Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Michigan, Missouri, New Jersey, New York, Ohio, Pennsylvania, Tennessee, West Virginia, Wisconsin and D.C. affected.

    There are 13 D.C. schools listed in the release:

    • Bridges Public Charter School
    • District of Columbia International School
    • DC Prep Anacostia Elementary Campus
    • DC Prep Anacostia Middle Campus
    • DC Prep Benning Elementary Campus
    • DC Prep Edgewood Elementary Campus
    • DC Prep Edgewood Middle Campus
    • Hope Community Charter School Tolson Campus
    • Ingenuity Prep Public Charter School
    • Learn D.C. Public Charter School
    • Richard Wright Public Charter School
    • Two Rivers Public Charter School 26th St Campus
    • Two Rivers Public Charter School 4th St Campus.

    No schools in Virginia or Maryland made the list — but the food was sent to restaurants, schools and other institutions between May and October.

    The federal agency said in a release that it will continue to update the list of retailers and schools that bought products with possible listeria contamination.

    WTOP’s Matt Small contributed to this report.

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    © 2024 WTOP. All Rights Reserved. This website is not intended for users located within the European Economic Area.

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    Emily Venezky

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  • Beds sold at Amazon, Walmart recalled due to collapse hazard

    Beds sold at Amazon, Walmart recalled due to collapse hazard

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    Nearly 138,000 platform beds sold at major retailers including Amazon and Walmart are being recalled across the U.S. and Canada because they can collapse, posing fall and injury risks.

    Utah-based importer CVB Inc. is recalling the Lucid-branded platform beds with upholstered square tufted headboards. According to Thursday notices from the U.S. Consumer Product Safety Commission and Health Canada, the beds can sag, break or collapse during use.

    To date, there have been 245 incidents of this occurring in the U.S., resulting in 18 related injuries such as contusions and bruises, the CPSC said. An additional 11 reports of “bed failures” have been reported in Canada, with no further injuries.

    People who have the recalled beds are urged to stop using them immediately and contact Lucid for a free replacement frame.

    According to Lucid, the recall covers a discontinued version of its platform beds, which the company says were manufactured between 2019 and 2021.

    While manufacturing ended several years ago, the now-recalled beds continued to be sold at major retailers through April 2024, the CPSC said. In addition to Amazon, Walmart and Lucid’s website, consumers may have also purchased the beds at Bed Bath & Beyond, eBay, Home Depot, Macys, Target.com, Wayfair and other retailers.

    About 137,000 of the recalled beds were sold in the U.S. and 890 in Canada, the CPSC said.

    The beds — which were made in Malaysia and come in twin, full, queen, king and cal-king sizes — can be identified with a white law label found on the back of the headboard. “Made For: CVB INC, 1525 W 2960 S, LOGAN, UT 84321” should be printed on it.

    People who have the recalled beds are urged to stop using them immediately and contact Lucid for a free replacement frame.

    Consumers will have to write the word “recalled” on the bed’s support rails with a permanent marker and send photos to Lucid. More information about getting a replacement can be found on Lucid’s recall page.

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    The Associated Press

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  • Stellantis recalls 1.5M Ram trucks to fix software bug

    Stellantis recalls 1.5M Ram trucks to fix software bug

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    DETROIT (AP) — Stellantis is recalling nearly 1.5 million Ram pickup trucks worldwide to fix a software problem that can disable the electronic stability control system.

    What You Need To Know

    • Stellantis is recalling nearly 1.5 million Ram pickup trucks worldwide to fix a software problem that can disable the electronic stability control system

    • The recall covers certain trucks from the 2019 and 2021 through 2024 model years, mostly in North America

    • Dealers will update software to fix the problem at no cost to owners, who will be notified by letters starting Oct. 3

    The recall covers certain trucks from the 2019 and 2021 through 2024 model years, mostly in North America.

    Stellantis said in a statement Saturday that the trucks may have anti-lock brake software that could inadvertently shut down the stability control, which manages the throttle and brakes to avoid skidding.

    If that happens, the company said the brakes would still work. Stellantis said it’s not aware of any crashes or injuries from the problem.

    U.S. safety standards require electronic stability control to work during nearly all phases of driving, the company says.

    Dealers will update software to fix the problem at no cost to owners, who will be notified by letters starting Oct. 3.

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    Associated Press

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  • Walmart recalls Great Value apple juice for arsenic

    Walmart recalls Great Value apple juice for arsenic

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    Walmart is recalling more than 9,500 cases of apple juice for elevated levels of inorganic arsenic, according to the U.S. Food and Drug Administration. 

    The FDA said the affected product could cause some health effects, but it’s unlikely to cause serious illness. Short-term exposure to inorganic arsenic can cause some symptoms, such as nausea, vomiting, bruising and numbness or burning sensations in the hands and feet, according to the FDA. Arsenic is present in places where food can be grown, so the FDA monitors arsenic levels in case they are above the normal standard. 

    The recall is for the Great Value brand 8-ounce, six-pack apple juice, which is packaged in PET plastic bottles with UPC 0-78742-29655-5.

    The affected packages of apple juice were sold in several states, including Alabama, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Maine, Michigan, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island South Carolina, Tennessee, Virginia, Vermont, West Virginia and Washington, D.C.

    It was also sold in Puerto Rico, the FDA said. 

     

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    Lydia Taylor

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  • Health officials recall some Boar’s Head deli meats amid listeria probe

    Health officials recall some Boar’s Head deli meats amid listeria probe

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    U.S. health officials Friday announced a recall of some Boar’s Head liverwurst and other deli meats as they investigate a listeria outbreak that has sickened nearly three dozen people and caused two deaths.

    What You Need To Know

    • U.S. health officials have announced a recall of some Boar’s Head liverwurst and other deli meats as they investigate a listeria outbreak

    • The outbreak has sickened nearly three dozen people and caused two deaths

    • Listeria can contaminate food and sicken people who eat it; symptoms include fever, muscle aches, nausea and diarrhea
    • Testing is underway to determine whether the company’s products are linked to the outbreak



    Boar’s Head Provisions Co. recalled its liverwurst because it may be tainted with the listeria bacteria, the U.S. Agriculture Department said. The company is also recalling additional deli meats that were produced on the same line and on the same day as the liverwurst.

    The USDA said a sample of Boar’s Head liverwurst from a Maryland store tested positive for listeria. The sample was from an unopened package, collected by the Maryland Department of Health as part of an investigation into the listeria outbreak.

    Testing is underway to determine if the liverwurst sample is connected to the outbreak, health officials said.

    The outbreak was first reported last week. As of Thursday, 34 people were sickened, with all but one hospitalized. Two people died.

    People most commonly reported eating deli-sliced turkey, liverwurst and ham, officials said.

    Listeria can contaminate food and sicken people who eat it. Symptoms include fever, muscle aches, nausea and diarrhea. It can be treated with antibiotics, but it is especially dangerous to pregnant women, newborns, the elderly and those with compromised immune systems.

    An estimated 1,600 people get listeria food poisoning each year and about 260 die, according to the Centers for Disease Control and Prevention.

    The Boar’s Head recall includes a number of products stamped with an August 10 sell-by date, including bologna, garlic bologna, beef bologna, beef salami, Italian Cappy-style ham and Extra Hot Italian Cappy-style ham. Also included is Steakhouse Roasted Bacon Heat and Eat, with a sell-by date of Aug. 15.

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    Associated Press

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  • Tesla layoffs, Cybertruck recalls and Serve Robotics goes public | TechCrunch

    Tesla layoffs, Cybertruck recalls and Serve Robotics goes public | TechCrunch

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    Welcome back to TechCrunch Mobility — your central hub for news and insights on the future of transportation. Sign up here — just click TechCrunch Mobility — to receive the newsletter every weekend in your inbox. Subscribe for free.

    Tesla is back in the news cycle and our crystal ball says it’s one of those long-term affairs. The week kicked off with layoffs — about 10% of its more than 140,000-person workforce — and CEO Elon Musk declaring he was going “balls to the wall” on autonomy. It ended with a Cybertruck recall. Cool cool.

    There’s lots more in the newsletter than just Tesla — although before we move on, do check out Sean O’Kane’s scoop about the company’s 1,800-mile Tesla Semi charging corridor program. Read on to catch up on Serve Robotics’ public market debut, a week of highs and lows for Waymo, and more.

    Let’s go! 

    A little bird

    While much of our focus is on startups and Silicon Valley, we do have some little birds in Washington, D.C.

    A little bird told us recently that federal regulators are getting close to publishing a Notice of Proposed Rulemaking on autonomous vehicle regulations, which would be the first set of federal guardrails proposed for the industry.

    Our source said the Federal Motor Carrier Safety Administration (FMCSA), which regulates commercial vehicles in the U.S., should have a proposal out by this summer, fall at the latest. We’re told that the federal ruling on AVs will likely establish a minimum safety standard for AVs to operate on public roads but that state governments could enforce stricter regulations within their own borders. We’ve been hearing about discussions and plans around federal AV regulations for years now. Have we finally started to make headway? We shall see. 

    Got a tip for us? Email Kirsten Korosec at kirsten.korosec@techcrunch.com, Sean O’Kane at sean.okane@techcrunch.com or Rebecca Bellan at rebecca.bellan@techcrunch.com. If you prefer to remain anonymous, click here to contact us, which includes SecureDrop (instructions here) and various encrypted messaging apps.

    Deal of the week

    money the station

    Serve Robotics, the Nvidia- and Uber-backed sidewalk robot delivery company, hit the public markets this week via a reverse merger. Serve expects its public debut to bring in around $40 million in gross proceeds, funding that will go toward R&D for future robots, manufacturing of new robots, geographic expansion and more.

    Serve’s goal is to increase its fleet from the 100 robots deployed today around Los Angeles to 2,000 robots across multiple U.S. cities by the end of 2025, via a partnership with Uber Eats. Serve has huge revenue ambitions, with plans to generate between $60 million and $80 million in annual revenue by that same deadline. In 2023, Serve brought in $207,545 in revenue at a loss of $1.5 million.

    FWIW, Uber and Nvidia are still shareholders, but their shares in the company are decreasing with this debut. Pre-IPO, Uber and Nvidia held a 16.6% stake and 14.3% stake, respectively. Once the offering closes, those stakes will change to 11.5% and 10.1%, per regulatory filings.

    Serve’s share price was $4 at market open on Thursday, and it closed that day at around $3.

    Other deals that got my attention …

    Found Energy, a startup that uses waste aluminum to generate heat and hydrogen, raised a $12 million seed round, but Tim De Chant’s story on the company is about so much more.

    Getir, a Turkish delivery company that was once worth $12 billion, is reportedly weighing asset sales and exits from non-core markets as investors put the pressure on to cut losses.

    Swtch Energy, a company building EV charging solutions for apartment buildings, raised $27.2 million in a Series B to expand its charging network and boost the tech behind its charging and energy management solutions. Blue Earth Capital led the round with participation from Alantra’s Energy Transition Fund Klima, Active Impact Investments and GIGA Investments Corp.

    Notable reads and other tidbits

    ADAS

    Mobileye has secured orders to ship 46 million of its EyeQ6 Light ADAS chips over the next few years to automakers. Multiple models launching this year will feature the chip, which promises to deliver improved sensing of wet roads, detection of and reaction to objects at a greater distance, and better ability to read key text phrases on road signs. TechCrunch had the chance to dig into this, and our main takeaways are that automakers will probably love this chip because it’s more powerful than Mobileye’s last chip, but it’s the same price.

    Autonomous vehicles

    Waymo has begun initial data collection and mapping in Atlanta, the company’s latest geographic win. The Alphabet-owned company didn’t say whether it plans to launch in the Georgian city or any other city it is mapping in, such as Washington, D.C., and Buffalo. Aside from San Francisco, Waymo has launched commercial robotaxi services in Los Angeles and Phoenix, with Austin planned for the end of this year.

    But with ups, come downs. Six Waymo vehicles also got caught blocking traffic to an on-ramp in San Francisco. The vehicles were caught between a construction zone and the on-ramp and had to pull over to await rescue. A spokesperson told TechCrunch that while Waymo does have the green light to go fully driverless on freeways in San Francisco, the company has not yet pulled the driver out.

    Electric vehicles, charging & batteries

    General Motors launched a home EV charger and vehicle-to-home (V2H) kit that lets a home pull energy from an EV battery in the event of a blackout. Customers in California, Florida, Texas, Michigan and New York can purchase today.

    Gogoro, the two-wheeler battery-swapping company, and TSMC, a global semiconductor company, are partnering to introduce 15 GoStations across Taiwan that use 100% clean energy. They’ll also be launching Gogoro’s scooter-sharing service in TSMC’s headquarter city, Hsinchu, and expanding the charging network in the city.

    TeslaCrunch

    We’ve been all over Tesla this week, so let’s dive in.

    The week started out with company-wide layoffs that affected at least 10% of the entire 140,000-person organization, with some teams seeing 20% of their staff gutted. Two high-profile executives departed Tesla as well: Drew Baglino, Tesla’s SVP of Powertrain and Energy, and Rohan Patel, VP of Public Policy and Business Development. Patel told TechCrunch he left because of “[b]ig overall changes” at the company that he declined to specify. In an email sent to the company, CEO Elon Musk said the cuts were necessary to increase productivity and prepare for Tesla’s “next phase of growth.”

    (Psssst! Don’t want to read about Tesla layoffs and what comes next? You can watch about it instead.)

    Many of those who were cut, sources say, were high performers who just happened to be working on lower-priority projects. Sources at Tesla also told TechCrunch the company made the cuts because it expects poor first-quarter earnings. Deliveries were subpar, and all those price cuts last year that continued early into 2024 likely had an effect on Tesla’s margins. Deliveries were down in Q1 year-over-year, despite the $200,000 Tesla spent on advertising on X, per our reporting.

    Which might be why Tesla ditched its EV inventory price discounts this week. On X, Musk said this move was in line with Tesla’s strategy to “streamline the whole Tesla sales and delivery system.”

    These changes in general, and the layoffs in particular, are made more stark by Tesla’s proxy statement that calls on the board to reinstate Musk’s $56 billion payout, which a Delaware judge earlier this year voided. In a huff, Musk threatened to reincorporate Tesla in Texas instead, and it appears that plan will also be put to the board soon.

    Meanwhile, on the charging front, Tesla is moving forward with its plan to build an electric big rig charging corridor stretching from Texas to California, despite being snubbed by a lucrative federal funding program that’s part of Biden’s Bipartisan Infrastructure law.

    Tesla this week also had to recall the 3,878 Cybertrucks that it has delivered to customers to date over faulty accelerator pedals that can get stuck. I know what you’re thinking. Finally we know how many Cybertrucks Tesla delivered.

    This week’s wheels

    I’ve been in a handful of new vehicles and I’m eager to share my thoughts, but we’re also running out of space this week. In the coming issues, we’ll have some takes on electric bikes, the 2024 Lexus LC 500h, the 2024 Mercedes-Benz eSprinter and more.

    See y’all next week!

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    Kirsten Korosec

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  • Kia is recalling over 427,000 Tellurides that might roll away while parked

    Kia is recalling over 427,000 Tellurides that might roll away while parked

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    Kia is recalling more than 427,000 of its Telluride SUVs due to a defect that may cause the cars to roll away while they’re parked.

    According to documents published by the National Highway Traffic Safety Administration, the intermediate shaft and right front driveshaft of certain 2020-2024 Tellurides may not be fully engaged. Over time, this can lead to “unintended vehicle movement” while the cars are in park — increasing potential crash risks.

    Kia America decided to recall all 2020-2023 model year and select 2024 model year Tellurides earlier this month, NHTSA documents show. At the time, no injuries or crashes were reported.

    Improper assembly is suspected to be the cause of the shaft engagement problem — with the recall covering 2020-2024 Tellurides that were manufactured between Jan. 9, 2019 and Oct. 19, 2023. Kia America estimates that 1% have the defect.

    To remedy this issue, recall documents say, dealers will update the affected cars’ electronic parking brake software and replace any damaged intermediate shafts for free. Owners who already incurred repair expenses will also be reimbursed.

    In the meantime, drivers of the impacted Tellurides are instructed to manually engage the emergency brake before exiting the vehicle. Drivers can also confirm if their specific vehicle is included in this recall and find more information using the NHTSA site and/or Kia’s recall lookup platform.

    Owner notification letters are otherwise set to be mailed out on May 15, with dealer notification beginning a few days prior.

    Subscribe to the Eye on AI newsletter to stay abreast of how AI is shaping the future of business. Sign up for free.

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    The Associated Press

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  • Faraday Future survives long enough to issue its first recall | TechCrunch

    Faraday Future survives long enough to issue its first recall | TechCrunch

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    Troubled EV startup Faraday Future has issued its first recall, covering all 11 vehicles it built last year, as it fights to hold onto its Los Angeles headquarters.

    The recall centers around a problem with the warning light for the airbags in Faraday Future’s FF91 SUV. The company apparently discovered that an error in the car’s software could prevent the warning light from turning on if there is a problem with the airbags.

    Faraday Future says it will “schedule concierge pick up, and redelivery, of the owners’ vehicles” to fix the software. So far, the earliest customers have been celebrities like Selling Sunset’s Jason Oppenheim, and (yes, seriously) singer Chris Brown.

    The recall comes as Faraday appears to be extremely low on cash. The landlord of its LA headquarters is trying to evict the startup after Faraday missed multiple lease payments. (A hearing is scheduled for early April.) Faraday has furloughed or cut the salaries of many of its remaining employees — cost-saving measures it recently extended through mid-to-late March, according to emails viewed by TechCrunch.

    Still, it is remarkable that after nearly 10 years and close to $4 billion in losses, Faraday Future has even made it to the point that it needs to issue a recall at all.

     

     

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    Sean O’Kane

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  • Maker of recalled sleep apnea machines agrees to halt sales in US

    Maker of recalled sleep apnea machines agrees to halt sales in US

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    The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the manufacturer nearly $400 million.

    Device maker Philips has recalled more than 5 million pressurized breathing machines due to risks that their internal foam can break down over time, leading users to inhale tiny particles and fumes while they sleep.

    The company first announced the problem in mid-2021, but efforts to repair or replace the machines have dragged on for years, frustrating patients in the U.S. and other countries.

    The Dutch manufacturing giant said it has agreed to a consent decree with the Food and Drug Administration and the Department of Justice. The deal has not yet been finalized and will have to be approved by a U.S. judge. Philips executives disclosed the tentative agreement during a quarterly earnings update.

    Under the agreement’s terms, Philips would continue servicing previously sold machines in the U.S., but couldn’t sell new ones until it meets corrective actions laid out by the FDA. Company executives said they have set aside $393 million for operational changes and upgrades needed to comply.

    The company promised it would put “safety and quality at the center of everything we do with a greater level of accountability,” Philips CEO Roy Jakobs told analysts and investors.

    The FDA’s website warns patients that the risks of ingesting the sound-dampening foam could include headache, asthma, allergic reactions and more serious problems. In November, the agency issued a new warning that the machines can overheat, in rare cases causing fires.

    The agency said it cannot comment on Philips’ announcement until a final agreement is “signed and filed with the court.”

    In 2022, the FDA took the rare step of ordering Philips to step up its outreach to customers about the recall including “clearer information about the health risks of its products.” At the time, the agency estimated only about half the people in the U.S. with affected machines knew they had been recalled.

    Customers trying to obtain refunds or new or refurbished devices from the company have reported months of delays.

    Most of the recalled devices are continuous positive airway pressure, or CPAP, machines. They force air through a mask to keep passageways open during sleep. The company has also recalled certain lines of ventilators and other breathing devices.

    Untreated sleep apnea can cause people to stop breathing hundreds of times per night, leading to dangerous drowsiness and increased heart attack risk. The problem is more common in men than women, with estimates ranging from 10% to 30% of adults affected.

    On Monday, Philips again pointed to company-commissioned studies suggesting that inhaling foam from its machines is “unlikely to result in appreciable harm” to patients. The company has discontinued several of the recalled models.

    The latest announcement does not resolve 675 personal injury lawsuits filed against the company over the devices. Those cases have been consolidated in a federal court in Pennsylvania.

    Philips faces similar legal challenges in Canada, Australia, Israel and Chile, according to the company’s update.

    ___

    The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group. The AP is solely responsible for all content.

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    Matthew Perrone | Associated Press

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  • Every Eye Drop and Gel Being Recalled From Target, CVS, Rite Aid | Entrepreneur

    Every Eye Drop and Gel Being Recalled From Target, CVS, Rite Aid | Entrepreneur

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    This article originally appeared on Business Insider.

    The FDA has warned consumers to immediately stop using and not buy 26 over-the-counter eye drops and gels that could potentially cause partial vision loss or blindness. Below is a list of all the products the FDA has told their manufacturer to recall.

    Agency investigators found unsanitary conditions and bacteria where the products were made, according to a safety alert from the FDA published on Friday, and said they had the potential to cause infections that could result in blindness.

    The FDA said on Friday that no adverse reactions had been flagged, but the products could pose “a potential heightened risk of harm” because drugs applied to the eyes bypass some of the body’s natural defenses.

    The products were marketed under the brands: Target Up&Up, CVS Health, Rite Aid, Leader (Cardinal Health), Rugby (Cardinal Health), and Velocity Pharma.

    Those who have signs or symptoms of an eye infection after using these products should speak to a healthcare provider or seek medical care immediately, the alert said.

    Eye drops and gels recalled by the FDA

    CVS Health:

    • Lubricant Eye Drops 15 ml (single pack)

    • Lubricant Eye Drops 15 ml (twin pack)

    • Lubricant Gel Drops 15 ml (single pack)

    • Lubricant Gel Drops 15 ml (twin pack)

    • Multi-Action Relief Drops 15 ml

    • Lubricating Gel drops 10 ml

    • Lubricant Eye Drops 10 ml (single pack)

    • Lubricant Eye Drops 10 ml (twin pack)

    • Mild Moderate Lubricating Eye Drops 15 ml (single pack)

    Rugby (Cardinal Health):

    Leader (Cardinal Health):

    Rite Aid:

    • Lubricant Eye Drops 15 ml (twin pack)

    • Lubricant Eye Drops 10 ml (twin pack)

    • Gentle Lubricant Gel Eye Drops 15 ml

    • Lubricant Gel Drops 15 ml

    • Lubricating Gel Drops 10 ml

    • Multi-Action Relief Drops 15 ml

    Target:

    • Up & Up Dry Eye Relief Lubricant Eye Drops 30 ml

    • Up & Up Extreme Relief Dry Eye 15 ml (single pack)

    • Up & Up Extreme Relief Dry Eye 30 ml (twin pack)

    Velocity Pharma:

    CVS, Rite Aid, and Target are pulling the drugs from shelves

    CVS, Rite Aid, and Target are removing the products from their shelves and websites after the FDA recommended on Wednesday all batches be recalled, the alert said.

    Products branded as Leader, Rugby, and Velocity may still be available in stores and online, the alert said, but they should not be purchased.

    A spokesperson for Rite Aid said: “Due to safety concerns identified by the FDA, we are removing the applicable Rite Aid branded products from our store shelves.”

    A CVS spokesperson told Insider in an email: “We’ve immediately stopped the sale in-store and online of all products supplied by Velocity Pharma within the CVS Health Brand Eye Products portfolio.” The spokesperson added that customers could return those products for a full refund.

    In a statement, Cardinal Health said: “Immediately upon being notified, we placed all identified impacted eye drop products in our inventory on hold and contacted Velocity Pharma, the supplier of the impacted eye drop products.

    “We are in the process of working with Velocity Pharma and FDA to initiate a recall of all impacted Rugby Laboratories and Cardinal Health Leader branded eye drop products to further safeguard public health and safety.”

    Target and Velocity Pharma did not immediately respond to requests for comment.

    In February, the Centers for Disease Control and Prevention and the FDA warned against two other eye-drop products, EzriCare Artificial Tears and Delsam Pharma’s Artificial Tears. The drugs were recalled over bacteria contamination, which was linked to four deaths and 14 cases of vision loss or eye removal.

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    Kim Schewitz

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  • More Than 60,000 Gun Safes Recalled After Parents Of 12-Year-Old Who Died Sue

    More Than 60,000 Gun Safes Recalled After Parents Of 12-Year-Old Who Died Sue

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    More than 60,000 gun safes were recalled nationwide on Thursday following dozens of reports that unauthorized people could open them, including a 12-year-old boy who died after allegedly accessing a gun inside, the U.S. Consumer Product Safety Commission announced.

    Illinois-based Fortress Safe recalled 61,000 gun safes after 39 reports that a flaw in the safes’ biometric feature made it seem like they were locked for unauthorized users, but actually remained in “default to open” mode. The recall urged safe owners to immediately stop using the biometric feature and to lock the safes with a key instead. It also told customers to contact Fortress Safe for information on how to receive a replacement safe.

    “The safes contain a biometric reader that allows unpaired fingerprints to open the safe until a fingerprint is programmed, allowing unauthorized persons, including children, to access hazardous contents, including firearms,” the company said.

    Carson Preston, 12, died of a gunshot wound after accessing a gun stored in a Fortress Safe gun safe, his family’s lawsuit alleges.

    Preston family via Claggett & Sykes Law Firm

    Fortress Safe said it was aware of a lawsuit filed this year alleging that a 12-year-old Nevada boy, Carson Preston, had died after accessing a gun from one of the company’s safes.

    According to a copy of the lawsuit obtained by HuffPost, Casey Preston, Carson’s father, had purchased the model 44B20 Fortress gun safe in March 2021 from the sporting goods store Scheels.

    On Jan. 28, the gun safe allegedly failed by allowing Carson, an unauthorized user, to access a handgun inside. According to the lawsuit, the safe was initially shipped in a state that allowed it to be opened with any fingerprint.

    As a result, Carson sustained a “lethal gunshot wound to the head,” according to the lawsuit.

    In a statement to HuffPost, Josh Dowling of Claggett & Sykes, the law firm representing the Preston family, said that “responsible gun owners should be able to rely on gun safes to protect their families.”

    “Our clients experienced every parent’s worst nightmare when their son was able to access their firearm because of the defective design of the Fortress gun safe,” Dowling said. “This recall is an important first step in holding Fortress responsible for placing a defective gun safe on the market. This recall reassures our clients that this was not their fault, and we hope it will prevent this type of tragedy from happening again.”

    The lawsuit also claims that Scheels had received reports and complaints from customers and individuals who said the gun safe was defective, but that the retailer continued to sell and advertise it.

    According to court documents obtained by HuffPost, Scheels denied those allegations, adding that the gun safe was “not in an unreasonably dangerous or defective condition” when it was sold. The company has filed a counterclaim against the Preston family, alleging that the child’s parents may be responsible for his death, and is seeking damages of more than $15,000 as well as attorneys’ fees.

    A representative for Scheels did not respond to HuffPost’s request for comment. Fortress Safe declined to comment.

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  • Family Dollar Recalls 301 Products: Tylenol, Advil, DayQuil | Entrepreneur

    Family Dollar Recalls 301 Products: Tylenol, Advil, DayQuil | Entrepreneur

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    Family Dollar has initiated a recall of hundreds of products, spanning over-the-counter medications, mouthwash, vitamins, and toothpaste, which were found by the Food and Drug Administration (FDA) to be improperly stored, the company stated on Wednesday in a release by the FDA.

    “These items were stored outside of labeled temperature requirements by Family Dollar,” per the release, and were then “inadvertently shipped” between June 1 and September 21. The recalled products were sold at Family Dollar stores in 23 different states.

    Although Family Dollar stated it has not received any notice of harm or illness related to the products, it is voluntarily issuing the recall “out of an abundance of caution.”

    The list of 301 products being recalled includes various well-known, over-the-counter medications including DayQuil liquid capsules, Advil PM, and Tylenol Extra Strength.

    Consumers who purchased any of the recalled products sold between June 1 and October 4 have the option to return the items to the place of purchase and receive a full refund, without the need for a receipt.

    The 23 states identified are Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Kansas, Louisiana, Mississippi, Montana, North Dakota, Nebraska, New Mexico, Nevada, Oklahoma, Oregon, South Dakota, Texas, Utah, Washington, and Wyoming.

    In a press release Wednesday, Family Dollar’s parent company, Dollar Tree, announced plans to build a new distribution center in West Memphis next year. The new facility, spanning 850,000 square feet, will feature comprehensive temperature control throughout the entire building.

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    Madeline Garfinkle

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  • Why Are There So Many Food Recalls? | Entrepreneur

    Why Are There So Many Food Recalls? | Entrepreneur

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    It’s never fun to find a foreign object in your food. And recently, there have been a series of recalls and contaminations of store-bought brands that have gone far beyond a stray hair.

    In the last few months alone, “extraneous materials” (metal fragments, rubber gaskets, insects) are among the top reasons for food recalls in the U.S., according to a report from ABC News.

    The annual Recall Index from brand protection firm Sedgwick found that, in 2022, the total number of units recalled by the FDA (which oversees 80 percent of the nation’s food supply) increased by 700% as compared to 2021. In 2022, there were 13 recalls by the U.S. Department of Agriculture’s Food Safety and Inspection Service (USDA).

    But so far in 2023, there have already been eight recalls by the USDA due to “possible foreign matter contamination.”

    Related: Trader Joe’s Is Recalling Cookies Because They May Contain Rocks

    However, the uptick in recalls doesn’t necessarily mean that the food we buy is “more contaminated” than it used to be.

    Keith Belk, director of the Center for Meat Safety and Quality at Colorado State University, told ABC that contamination detection has significantly improved in recent years, contributing to the number of recalls. Factors like new investigation tools, heightened monitoring by the FDA, and third-party testing companies have also contributed to the rising number of recalls being reported.

    Also, the FDA acknowledges that some level of contamination may be expected.

    “It is economically impractical to grow, harvest, or process raw products that are totally free of non-hazardous, naturally occurring, unavoidable defects,” the agency notes in its handbook.

    “The thing is, there’s never going to be a day where there’s zero risk associated with consuming a food product,” Belk told ABC.

    To stay on top of the risks, bookmark FoodSafety.gov and Recalls.gov.

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    Madeline Garfinkle

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  • Marijuana products recalled in Arizona for possible mold contamination – Medical Marijuana Program Connection

    Marijuana products recalled in Arizona for possible mold contamination – Medical Marijuana Program Connection

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    PHOENIX – Several marijuana dispensaries in Arizona are voluntarily recalling some products due to possible fungal contamination. 

    The Arizona Dept. of Health Services says two strains produced by TRU Infusion – Zombie Cookies and Peach Gas – are being recalled after samples tested positive for Aspergillus.

    So far, no illnesses have been reported. Health officials say there were errors in the testing results, which may have led to false negative results for contaminants.

    “Once ADHS discovered the potential contamination, they contacted the facility that produced the products,” health officials said. “The licensee took immediate action to work with all distribution and retail partners to remove any potentially impacted products from store shelves.”

    The affected batch numbers are 1110R29ZMBC and 1021R32PG.

    Some marijuana products recalled in Arizona

    What is Aspergillus?

    According to the Mayo Clinic, Aspergillus is a mold that exists both indoors and outdoors.

    “Most strains of this mold are harmless, but a few can cause serious illnesses when people with weakened immune systems, underlying lung disease or asthma inhale their fungal spores,” read a portion of the Mayo Clinic’s website.

    Aspergillus, according to the Cleveland Clinic, can cause a disease known as Aspergillosis.

    “In certain people, Aspergillus can cause allergic reactions, chronic lung conditions and invasive disease that spreads to your brain, kidneys, lungs or other organs,” read a portion of the…

    Original Author Link click here to read complete story..

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  • Peloton Recalls 2.2 Million Bikes Due To Safety Hazards | Entrepreneur

    Peloton Recalls 2.2 Million Bikes Due To Safety Hazards | Entrepreneur

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    On Thursday, Peloton issued a voluntary recall of its original Bike (model number PL-01) sold between January 2018 and May 2023. The U.S. Consumer Product Safety Commission (CPSC) issued a subsequent warning, and told consumers to cease using the recalled model “immediately.”

    Peloton said the recall is due to the vulnerability of the seat post, which has been reported to “break unexpectedly during use,” and poses serious risks of falling or injury. As of April 30, Peloton was notified of 35 instances of the seat post breaking during use, 13 of which led to lacerations, bruises, and in one case a fractured wrist, per the CPSC report.

    Related: Peloton Bikes Will Now Be Sold on Amazon as Company Reports $1 Billion Loss

    The recall applies to the Peloton original Bike sold in the U.S., which spans about 2.2 million bikes. The company is offering free seat post replacements that can be self-installed. No refunds will be issued as part of the recall.

    “Our commitment to Member safety is unwavering,” Peloton said in a statement. “For Peloton, it was important to proactively engage the CPSC to address this issue. We worked cooperatively with them to identify today’s approved remedy.”

    Peloton’s popularity boomed during the pandemic — sales surged by 172% in Q4 2020, and the company reached over one billion in total revenue for the second quarter of 2021. However, Peloton’s profitable reign was relatively short-lived, and when lockdown restrictions eased, so did sales — by the end of 2022, the company’s revenue was down to 678.7 million.

    This is the second injury-related recall for the exercise equipment company. In May 2021, Peloton recalled about 125,000 of its Tread+ treadmills following the death of a six-year-old child. In January 2023, the company agreed to pay $19 million in civil penalties for “knowingly failing” to report hazards associated with Tread+, noting that Peloton was informed of several safety issues related to the equipment between 2018 and 2019, but did not immediately report the hazards to CPSC.

    Related: Peloton Workers Were Told to Cover Up Flaking Paint, Rust on Bikes Before Shipping Them to Customers

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    Madeline Garfinkle

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  • Tesla Driver Killed After Plowing Into Fire Truck Parked On California Freeway

    Tesla Driver Killed After Plowing Into Fire Truck Parked On California Freeway

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    WALNUT CREEK, Calif. (AP) — A Tesla driver was killed and a passenger was critically injured Saturday when the car plowed into a fire truck that was parked on a Northern California freeway to shield a crew clearing another accident, fire officials said.

    Four firefighters who were in the truck when it was struck on Interstate 680 were treated for minor injuries, said Tracie Dutter, assistant chief of the Contra Costa County Fire Protection District.

    The driver was declared dead at the scene, Dutter said. The car needed to be cut open to remove the passenger, who was taken to the hospital.

    Photos showed the front end of the car was crushed and the $1.4 million ladder truck was damaged.

    California Highway Patrol Officer Adam Lane said it was not clear whether the driver may have been intoxicated or whether the Tesla Model S was operating with automation or driving assistance features.

    Dutter said the truck had its lights on and was parked diagonally on northbound lanes of the freeway to protect responders to an earlier accident that did not result in injuries.

    The fatal accident occurred around 4 a.m., and it took several hours to clear the freeway. The firetruck had to be towed away.

    The Model S was among the nearly 363,000 vehicles Tesla recalled on Thursday because of potential flaws in its “Full Self-Driving” system. While the recall is aimed at correcting possible problems at intersections and with speed limits, it comes amid a broader investigation by U.S. safety regulators into Tesla’s automated driving systems.

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  • Tyson Recalls Ground Beef for Having ‘Mirror-Like Material’ In It

    Tyson Recalls Ground Beef for Having ‘Mirror-Like Material’ In It

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    Texas beef buyers, beware.

    Tyson Foods Inc is recalling 93,697 pounds of raw ground beef, saying it may be contaminated with a hard “mirror-like material,” according to the USDA.

    The beef was produced on November 2 and distributed to retail locations in Texas, including H-E-B grocery stores. After the company received several customer complaints about glass in their beef, they contacted the Food Safety and Inspection Service (FSIS) and the product was cleared from the shelves.

    Related: Tyson Foods Takes a Lickin’ and Keeps on Tickin’ Lower

    Here’s a list of the products recalled.

    • 10-lb. chubs containing “HILL COUNTRY FARE GROUND BEEF 73% LEAN/ 27% FAT with BEST BEFORE OR FREEZE BY: NOV 25, 2022.”
    • 5-lb. chubs containing “HILL COUNTRY FARE GROUND BEEF 73% LEAN/ 27% FAT with BEST BEFORE OR FREEZE BY: NOV 25, 2022.”
    • 5-lb. chubs containing “H-E-B GROUND CHUCK GROUND BEEF 80% LEAN/ 20% FAT.”

    Thankfully, the FSIS says there have been “no confirmed reports of adverse reactions due to consumption of these products.”

    The agency urges anyone who thinks they may be ill or injured due to consumption to contact a doctor.

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    Jonathan Small

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