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Tag: product recall

  • Ford recalls nearly 1.9 million older Explorer SUVs over loose trim pieces that may increase risk of crash

    Ford recalls nearly 1.9 million older Explorer SUVs over loose trim pieces that may increase risk of crash

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    Ford is recalling nearly 1.9 million Ford Explorer SUVs in the U.S. because of loose clips that could detach, allowing the windshield trim panels to fly off while the vehicle is traveling at highway speeds. 

    The recall covers Explorers from the 2011 through 2019 model years.

    The recall concerns A-pillar retention clips that hold the trim that covers the vehicle’s roof supports by the windshield. “The A-pillar trim retention clips may not be properly engaged, allowing the trim to detach,” Ford Motors stated in a notification it sent to the the National Highway Traffic Safety Administration (NHTSA) acknowledging the recall. Flying parts could increase the risk of a crash, the agency said, both for the vehicle’s driver and others on the road. 

    Ford’s recall comes a year after the NHTSA first announced it was investigating the sports utility vehicles after receiving 164 complaints about the trim pieces detaching on 2011 through 2019 Explorer SUVs. There are no reports of crashes or injuries relating to the loose parts, the agency noted at the time.

    Remedy to come

    The company encourages owners of the recalled vehicles to contact dealers for an inspection when parts are available. Ford dealers will inspect and replace the A-pillar trim for free, if needed, according to the recall. 

    Car owners will receive a letter about the safety risk after March 13, 2024, with a second letter to follow when a remedy is available.

    Consumers with questions about their vehicles can contact Ford customer service at 1-866-436-7332. Ford’s number for this recall is 24S02. 

    Consumers can also reach the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or visit www.nhtsa.gov.

    — With reporting by the Associated Press.

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  • More than 580,000 beds sold at Walmart, Wayfair and Overstock recalled because they can break or collapse

    More than 580,000 beds sold at Walmart, Wayfair and Overstock recalled because they can break or collapse

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    More than 580,000 beds sold at retailers including Walmart and Wayfair are under recall because they can break, sag or collapse while in use, posing the risk of falls and injuries. 

    The bed’s manufacturer, Home Design, has received 128 reports of the beds sagging, breaking or collapsing, resulting in 36 injuries, according to a January 18 recall notice from the U.S. Consumer Product Safety Commission. The recall covers about 527,000 beds sold in the U.S. and roughly 56,000 units sold in Canada. 

    The recall encompasses several different models and sizes of upholstered low-profile standard and platform beds from Silver Lake, Indiana-based Home Design. Both Home Design and the CPSC are urging consumers with the recalled beds to stop using them immediately, as well as to contact the company for free replacement slats and side rails.

    80002.png
    One of the models recalled because of the risk that the bed could collapse or sag during use. 

    Consumer Product Safety Commission


    Consumers can determine if their bed is being recalled by checking the list of affected models and corresponding part number, which can be found on both the CPSC’s Thursday recall notice and on Home Design’s website. 

    The recall involves:

    •  All Home Design Part number 80002 Tufted Upholstered Low Profile Standard Beds, a gray, warm gray, or blue bed frame with standard supports requiring a box spring, available in twin, full, queen and king size.
    • Part number 80032 Tufted Upholstered Low Profile Standard Beds, a gray or beige bed frame with standard supports requiring a box spring, available in twin, full, queen and king size.
    • Part number 80055 Tufted Upholstered Low Profile Standard Beds, a silver gray, gray, or black bed frame with standard supports requiring a box spring, available in king size.
    • Part number 80071 Tufted Upholstered Low Profile Platform Beds, a gray, beige, or black bed frame with platform supports which does not require a box spring, available in twin, full, queen or king.
    • Part number 80053 Tufted Upholstered Low Profile Platform Beds, a warm gray bed frame with platform supports which does not require a box spring. Part number 80053 does not have a center support leg halfway along the side rail.

    To receive the free repair kit, consumers will need to email Home Design photos of the bed or proof of purchase as well as the headboard’s “law label.”

    The recalled beds, which were manufactured in Malaysia, were sold at Wayfair, Walmart.com and Overstock.com between July 2018 and November 2023. Prices ranged from $100 to $300.

    —With reporting by the Associated Press.

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  • Quaker Oats expands granola product recall due to salmonella risk

    Quaker Oats expands granola product recall due to salmonella risk

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    Quaker Oats expands granola product recall due to salmonella risk – CBS News


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    Quaker Oats has expanded its list of recalled products because they may be contaminated with salmonella. The newly-recalled products include various Cap’n Crunch cereals and Gatorade protein bars.

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  • Quaker Oats recalls more granola products due to salmonella risk

    Quaker Oats recalls more granola products due to salmonella risk

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    Quaker Oats expands granola product recall


    Quaker Oats expands granola product recall due to salmonella risk

    00:19

    Quaker Oats is expanding a prior recall to include additional cereals, granola bars and snacks sold across the U.S. because they could be contaminated with salmonella.

    The recalled products are sold throughout the 50 states, Puerto Rico, Guam and Saipan, Quaker Oats said in a notice posted Thursday by the U.S. Food and Drug Administration. See here for a full list of the recalled items, including those listed in an initial recall in mid-December. 

    Salmonella can cause serious illness if it enters the bloodstream, especially in young children, elderly people and those with weakened immune systems. The organism causes an estimated 1.3 million infections in Americans every year, resulting in an average of more than 26,000 hospitalizations and 420 deaths, CDC data shows.

    Symptoms of infection usually occur within 12 hours to three days after eating contaminated food and include diarrhea, fever, nausea and abdominal cramps.

    The recall includes Quaker Chewy Granola Bars, Cap’n Crunch Bars and select Cap’n Crunch cereals and oatmeal, Quaker Chewy Granola Breakfast cereals and Quaker Oatmeal Squares, Gamesa Marias Cereal, Gatorade Peanut Butter Chocolate Protein Bars, Munchies Munch Mix, and snack boxes that include these products, according to the Chicago-based company, a division of PepsiCo. 

    The recall does not include Quaker Oats, Quaker Instant Oats, Quaker Grits, Quaker Oat Bran, Quaker Oat Flour and Quaker Rice Snacks.

    Consumers are urged to check their pantries for the recalled products and dispose of them. Additionally, consumers with any of the recalled products can contact Quaker Consumer Relations (9 a.m. – 4:30 p.m. CST, Mon.-Fri.) at 1-800-492-9322 or visit www.QuakerRecallUSA.com for additional information or product reimbursement.

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  • Benny T’s dry hot sauces recalled over undisclosed wheat allergy risk

    Benny T’s dry hot sauces recalled over undisclosed wheat allergy risk

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    Vesta Fiery Gourmet Foods is recalling several types of its Benny T’s dry hot sauces because the product labels do not disclose that the sauces contain wheat flour, a potential allergen.  

    The recall comprises five flavors of chile pepper-based dry sauces that come in 1.5-ounce jars, the Raleigh, North Carolina-based food company said Monday in a statement on the Food and Drug Administration’s site. People with allergies or severe sensitivities to wheat could “face the risk of serious or life-threatening allergic reaction if they consume the dry sauces,” the company said. 

    The FDA has not received any reports of illnesses linked to the sauces. 

    The affected products are as follows:  

    Product

    Size

    UPC

    Benny T’s Vesta Ghost

    1.5 Ounce

    7 94571 99498 0

    Benny T’s Vesta Hot

    1.5 Ounce

    7 94571 99497 3

    Benny T’s Vesta Reaper

    1.5 Ounce

    7 94571 99490 4

    Benny T’s Vesta Scorpion

    1.5 Ounce

    7 94571 99491 1

    Benny T’s Vesta Very Hot

    1.5 Ounce

    7 94571 99499 7

    The recalled sauces were distributed across the U.S., between Oct. 1, 2023 and Jan. 4, 2024, and include the following lot numbers and expiration dates: FX001500 (expiration date 09/2024); FX001582 (expiration date 09/2024); NDC 0078-0110-22. The products were sold primarily online, as well as in retail stores and deli cases, it said.

    The FDA advises consumers who have purchased the condiments not to use them and to discard them. Those with questions about the recall can contact a Benny T’s brand representative, Chris Tuorto, at 919-656-7688 on weekdays between 8 a.m. and 9 p.m. Eastern.

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  • Nearly 5 million blenders recalled over broken blades, overheating issues

    Nearly 5 million blenders recalled over broken blades, overheating issues

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    Nearly 5 million blenders recalled over broken blades, overheating issues – CBS News


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    About 4.8 million blenders made by BlendJet Inc. are being recalled because of reports that the blades are breaking off, as well as reports the blenders are overheating and causing fires.

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  • Almost 5 million blenders sold at Costco, Target and Walmart are recalled because blades are breaking off

    Almost 5 million blenders sold at Costco, Target and Walmart are recalled because blades are breaking off

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    BlendJet Inc. is recalling about 4.8 million portable blenders sold at Costco, Target and Walmart after receiving reports of blades breaking off as well as the product overheating or catching fire, resulting in dozens of injuries. 

    The Benicia, California-based company has heard of 329 incidents in which BlendJet 2 Portable Blenders’ blades broke off while in use, and an additional 17 reports of overheating or fires that have resulted in property damage claims of roughly $150,000, according to a notice posted Thursday by the Consumer Product Safety Commission.

    BlendJet has also received 49 reports of minor burn injuries and one laceration injury. 

    “While none of the reported incidents resulted in serious injury or significant property damage, out of an abundance of caution, our company updated the base of the BlendJet 2 to feature thicker blades and an improved electrical configuration,” BlendJet said in a news release. The updates were incorporated many months ago, it added.

    Consumer Reports offered a somewhat different take, noting that it began raising safety concerns to the CPSC and BlendJet about the recalled blenders in August.  “In one complaint involving an injury, a consumer reported that the blender started smoking while plugged in, and the complainant’s son reportedly burned his finger when unplugging it,” CR stated. 

    “BlendJet should get the word out about this recall as much as possible in the new year, and we urge the company to offer people a refund if they aren’t comfortable getting a replacement,” William Wallace, CR’s associate director of safety policy, said on Thursday in an emailed statement.

    415191825-786737796830669-4266613260418338038-n.jpg

    U.S. Consumer Product Safety Commission


    Manufactured in China, the recalled product was sold at stores nationwide and online from October 2020 through November 2023 for between $50 and $75. Offered in a variety of colors and designs, the recalled blenders contain serial numbers where the first four digits range between 5201 to 5542. Consumers can also go here to identify the blenders.

    Consumers are urged to stop using the blenders and to contact BlendJet for a free base unit replacement, according to the CPSC notice. People who bought the recalled product will have to remove and cut up the base’s rubber seal and email or upload a photo to the company’s website.

    BlendJet 2 blenders with serial numbers that start with “5543” or higher are not being recalled as they already have updated components, BlendJet stated. 

    Beyond the 4.8 million recalled blenders sold in the U.S., another roughly 117,000 were sold in Canada.

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  • Company faces lawsuit over lead-tainted applesauce

    Company faces lawsuit over lead-tainted applesauce

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    Company faces lawsuit over lead-tainted applesauce – CBS News


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    Wanabana, one of the companies that has recalled applesauce pouches due to lead contamination, is facing a possible class action lawsuit over the tainted products. Meg Oliver reports.

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  • Tesla recalls more than 120,000 vehicles because doors can unlatch in a crash

    Tesla recalls more than 120,000 vehicles because doors can unlatch in a crash

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    Tesla is recalling 120,423 vehicles because the doors can unlatch and open in a crash, heightening the risk of injury, according to safety regulators. 

    The issue affects some 2021-2023 Model S and Model X vehicles, the National Highway Traffic Safety Administration (NHTSA) said in a filing. Engineers at Tesla, a maker of electric cars, discovered the defect on December 6 while conducting side-impact tests on vehicles, according to the agency. 

    As of December 14, Tesla was not aware of any warranty claims or injuries related to the problem. 

    Tesla has released a free software update to resolve the problem, and the automaker also plans to notify car owners by mail on Feb. 17, 2024. For more information, people may contact Tesla customer service at (877) 798-3752 or NHTSA at (888) 327-4236, as well as visit the agency’s website.

    Autopilot recall

    Tesla last week also recalled more than 2 million vehicles across the company’s model lineup — nearly all of its cars on the road — to fix a defective system that’s supposed to ensure drivers are paying attention when they use Autopilot. That followed two-year probe by NHTSA into a series of crashes that happened while the Autopilot partially automated driving system was in use. 


    Tesla recalling more than 2 million vehicles to fix a safety issue with its autopilot feature

    02:28

    To address that problem, Tesla sent drivers a software update that installs alerts designed to better ensure that drivers are fully aware and paying attention even when Autopilot is engaged. 

    Specifically, the update will address Tesla Autosteer function, one of two Autopilot features. Autosteer is designed to keep vehicles on track and in their lanes on freeways. The update limits where Autosteer can be used, depending on conditions in a vehicle’s surrounding environment. It will alert drivers that Autosteer is unengaged, according to the recall documents. 

    —The Associated Press and CBS News’ Megan Cerullo contributed to this report.

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  • Honda recalls 2.5 million cars because of stalling risk. See if your car is one of them.

    Honda recalls 2.5 million cars because of stalling risk. See if your car is one of them.

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    Toyota recalls 1 million vehicles


    Toyota recalls 1 million vehicles over air bag issue

    00:27

    Honda is recalling more than 2.5 million cars because the fuel pump inside the fuel tank may fail, causing the vehicles to stall while driving and increasing the risk of a crash, according to the National Highway Traffic Safety Administration.

    The fuel pump module in the recalled vehicles will be replaced by dealers at no charge, NHTSA said on Wednesday. Owners can also contact Honda customer service at (888) 234-2138. The automaker will start notifying owners of the recall by mail on February 5, the government agency said. 

    The recall comes only one day after Honda recalled about 106,000 CR-V hybrid sport utility vehicles because of a battery cable problem that can raise the risk of a fire during an accident. In the latest recall, some CR-V hybrids are also affected by the fuel pump issue. 

    Acura models under recall

    • Acura ILX, 2018-2020
    • Acura MDX, 2018-2020
    • Acura MDX hybrid, 2018-20
    • Acura NSX, 2017-2020
    • Acura RDX, 2018-2020
    • Acura RLX, 2018-2020
    • Acura TLX, 2018-2020

    Honda Accord models

    • Honda Accord, 2018-2020
    • Honda Accord hybrid, 2017-2020

    Honda Civic models

    • Honda Civic, 2018-2020
    • Honda Civic Type-R, 2018-2020

    Honda CR-V models

    • Honda CR-V, 2018-2020
    • Honda CR-V Hybrid, 2020

    Honda Odyssey, Ridgeline and other models

    • Honda Odyssey, 2018-2020
    • Honda Ridgeline, 2018-2020
    • Honda Clarity plug-in hybrid, 2018-2019
    • Honda Fit, 2018-2019
    • Honda HR-V, 2018-2020
    • Honda Insight, 2019-2020
    • Honda Passport, 2019-2020

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  • Coca-Cola issues soda recall over

    Coca-Cola issues soda recall over

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    Coca-Cola issues soda recall over “foreign material” – CBS News


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    Coca-Cola this week recalled about 2,000 cases of Diet Coke, Sprite and Fanta Orange because they may contain “foreign material.” Read more here.

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  • Salmonella-linked cantaloupe recall expands

    Salmonella-linked cantaloupe recall expands

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    Salmonella-linked cantaloupe recall expands – CBS News


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    At least 117 people in 34 states have been sickened in a salmonella outbreak linked to cantaloupe, the U.S. Centers for Disease Control and Prevention said Thursday.

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  • What to know about the widening cantaloupe recall over deadly salmonella risks

    What to know about the widening cantaloupe recall over deadly salmonella risks

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    Consumers who eat cantaloupe are advised to be on high alert following a spate of government warnings over a deadly salmonella outbreak linked to the fruit. 

    U.S. health officials have ordered sweeping recalls of potentially contaminated whole and pre-sliced cantaloupes over the past few weeks, in addition to urging consumers on Thursday to toss out any products containing the melon, recall notices from officials show. The flurry of warnings has prompted major grocery sellers such as Kroger, Trader Joe’s and Walmart to continue removing products containing the melon from store shelves. 

    Bacteria-harboring cantaloupes have been linked to at least 117 illnesses, including 61 hospitalizations and two deaths across 34 U.S. states, and those numbers could grow, the Centers for Disease Control and Prevention said Thursday in a statement. 

    Here’s what to know about the latest rash of cantaloupe recalls, and how to know if you should save or toss that fruit in your fridge. 

    What is happening? 

    Following an outbreak of severe bacterial infections linked to the fruits, the CDC is warning consumers to steer clear of pre-cut cantaloupe if they are unsure of whether it is from a distributor whose product has been recalled.

    The guidance follows previous orders by U.S. health officials to recall whole cantaloupes from several brands, including Malichita and Rudy, which prompted several nationwide grocery chains to recall their own products containing pre-cut cantaloupes. Most recently, Sprouts Farmers Market and Trader Joe’s on Wednesday pulled select fresh-cut products made from whole cantaloupes off their shelves, according to an FDA notice.

    Cut Fruit Express of Inver Grove Heights, Minnesota, on Wednesday recalled products containing cantaloupe, including Caribou Coffee Fruit Mix CHPG 6.5oz; Cut Fruit Express Brand 6.5oz, 15oz, 16oz, 32oz packages of fruit mix; and food service packages of 5lb-tray, 10lb-bag, 25lb-Pail, all of which could be contaminated with salmonella.

    Which products are affected? 

    Whole fresh cantaloupes with Malichita, Rudy, “4050” and “Product of Mexico/produit du Mexique” labels are not safe to consume and should be thrown away, the FDA said

    In addition, products containing pre-cut cantaloupe such as fruit salads may pose a salmonella risk to consumers, according to the agency. Since November, there have been at least three waves of recalls issued over pre-cut cantaloupe by major grocery stores, including Kroger, Trader Joe’s, Sprouts Farmer Market, Aldi, and Walmart, according to the FDA. 

    What should I do if I don’t know my cantaloupe’s brand? 

    The FDA is advising consumers to toss out any cantaloupe that cannot be identified by brand. 

    “If you cannot tell if your cantaloupe, including pre-cut cantaloupe or products containing pre-cut cantaloupe is part of the recall, do not eat or use it and throw it away,” the agency said Thursday in a statement. 

    In addition to throwing out the melon, that FDA advises people to wash any surfaces that may have come into contact with the cantaloupe, using hot, soapy water or a dishwasher, the agency said. 

    What is Salmonella? 

    Salmonella, or salmonellosis, is a bacterial infection that affects the intestinal tract, according to the Mayo Clinic, a nonprofit medical research center. Symptoms include diarrhea, fever and stomach cramps, which usually begin between eight and 72 hours after exposure to the bacteria.

    Not everyone who contracts salmonella experiences symptoms, according to the Mayo Clinic. Children under age five, the elderly and those with weakened immune systems are more at risk of developing severe illnesses that require medical care or hospitalization. 

    People who get salmonella should rest and drink plenty of fluids to avoid dehydration, according to the Cleveland Clinic. The infection usually resolves on its own in a few days.  

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  • Honda recalls more than 300,000 Accords and HR-Vs over missing seat belt piece

    Honda recalls more than 300,000 Accords and HR-Vs over missing seat belt piece

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    Honda is recalling several hundred thousand 2023-2024 Accord and HR-V vehicles due to a missing piece in the front seat belt pretensioners, which could increase injury risks during a crash.

    According to notices published by Honda and the National Highway Traffic Safety Administration earlier this week, the pretensioners — which tighten seat belts in place upon impact — may be missing the rivet that secures the quick connector and wire plate. This means that passengers may not be properly restrained in a crash, regulators said.

    The NHSTA credited the issue to an error made during assembly. More than 300,000 Accords and HR-Vs are potentially affected.

    Dealers will inspect and replace the seat belt pretensioner assemblies as necessary, free of charge, the NHTSA said in its notice.

    As of Nov. 16, Honda had received seven warranty claims, but no reports of injuries or deaths related to the faulty pretensioners, according to documents published by the NHTSA.

    Those who have already paid for these repairs at their own expense may also be eligible for reimbursement.

    Notification letters will are set to be sent via mail to registered owners of the affected vehicles starting Jan. 8, 2024. For more information about the recall, consumers can visit the NHTSA and Honda’s and online recall pages.

    Earlier this month, Honda recalled almost 250,000 vehicles in the U.S. because their bearings can fail, causing the engines to stall and increasing the risk of a crash. The company said in documents they had 1,450 warranty claims due to the problem, but no reports of injuries.

    In June, Honda recalled nearly 1.2 million cars because the rearview camera images may not appear on the dashboard screen. 

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  • Wilcox Ice Cream recalls all flavors due to possible listeria contamination

    Wilcox Ice Cream recalls all flavors due to possible listeria contamination

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    Wilcox Ice Cream is recalling all flavors of Wilcox brand ice cream, yogurt and ice cream bars, as well as Leonardo’s brand gelato, because the products could be contaminated with listeria, the company said.

    The New Hampshire Department of Health found that the Arlington, Vermont, ice cream maker’s Super Premium Mint Chocolate Chip tested positive for the bacteria during routine testing in September. 

    “As part of our investigation, we determined that preliminary testing showed that the ice cream mix purchased to make our products may contain listeria monocytogenes,” Wilcox said in a recall notice posted by the Food and Drug Administration. 

    The organism can cause serious, and sometimes fatal, infections in young children, frail or elderly people, as well as in others with weakened immune systems. While healthy people may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infections can also cause miscarriages and stillbirths in pregnant women.

    No illnesses or injuries related to the recalled products have been reported to date, Wilcox said. 


    Soft serve ice cream recalled due to listeria outbreak

    00:27

    Separately, two people were hospitalized in a listeria outbreak linked to ice cream made by The Ice Cream House of Brooklyn, New York, which issued separate recalls in August and September.

    The latest recall involves Wilcox-made products that were distributed in retail stores and co-ops in four states: Massachusetts, New Hampshire, New York and Vermont.

    Recalled ice cream.

    U.S. Food and Drug Administration


    In addition to that flavor, the company is recalling all products made at its facility with best by/sell by dates of September 14, 2024, to November 14, 2024: 

    • Wilcox SUPER premium Salted Carmel Brownie 1.5 Quart 043726152
    • Wilcox SUPER PREMIUM Chocolate 1.5 Quart 04372601502
    • Wilcox SUPER PEREMIUM Maple Cream 1.5 Quart 04372601510
    • Wilcox SUPER PREMIUM Maple Walnut 1.5 Quart 04372601511
    • Wilcox SUPER PREMIUM Mint Chunk 1.5 Quart 04372601512
    • Wilcox SUPER PREMIUM Super Jave 1.5 Quart 04372601516
    • Wilcox SUPER PREMIUM Vanilla 1.5 Quart 04372601519
    • Wilcox SUPER PREMIUM Chocolate 1.5 Quart 04372601502
    • Wilcox SUPER PREMIUM Maple Cream Pint 0437260110
    • Wilcox SUPER PREMIUM Maple Walnut Pint 04372601611
    • Wilcox SUPER PREMIUM Mint Chunk Pint 0437261612
    • Wilcox SUPER PREMIUM Super Java Pint 04372601616
    • Wilcox SUPER PREMIUM Vanilla Pint 04372601619
    • Wilcox SUPER PREMIUM Salted Caramel Brownie Pint 04372601620

    Wilcox’s Premium Yogurt Line with Best By/Sell By November 5, 2024, November 6, 2024, November 26, 2024, and November 27, 2024:

    • Wilcox Yogurt – Vanilla Pint 04372601520
    • Wilcox Yogurt – Maple Cream Pint 04372600698
    • Wilcox Yogurt – Black Raspberry Pint 04372600695 

    Wilcox Ice Cream 8-oz Ice Cream Bars with Best By/Sell By September 15, 2024, through November 14, 2024:

    • Wilcox Ice Cream Bar (Dairy Based) – Vanilla 043726005041
    • Wilcox Ice Cream Bar (Dairy Based) – Black Raspberry 043726005065
    • Wilcox Ice Cream Bar (Dairy Based) – Espresso 043726005072
    • Wilcox Ice Cream Bar (Dairy Based) – Maple Cream 043726005096
    • Wilcox Ice Cream Bar (Dairy Based) – Pumpkin 043726005010
    image-2-233.jpg
    Recalled gelato.

    FDA


    Leonardo’s Gelato Pints and 4-ounce cups with Best By/Sell By August 28, 2024, through November 14, 2024:

    • Leonardo’s Gelato – Maple Gelato Pint 816439000055
    • Leonardo’s Gelato – Sam’s Creamy Chocolate Chip Pint 81643900019
    • Leonardo’s Gelato – Chocolate Gelato Pint 81643900005
    • Leonardo’s Gelato – Salted Caramel Gelato Pint 04372601701
    • Leonardo’s Gelato – Hazelnut Gelato Pint 04372601703
    • Leonardo’s Gelato – Mint Chocolate Chip Pint 816439000050
    • Leonardo’s Gelato – Chocolate Gelato 4-ounce cup 81643900028
    • Leonardo’s Gelato – Sam’s Chocolate Chip 4-ounce cup 81643900040
    • Leonardo’s Gelato – Vermont Maple Gelato 4-ounce cup 81643900056
    • Leonardo’s Gelato – Mint Chocolate Chip 4-ounce cup 81643900041

    People should not consume the recalled products.

    Those who purchased affected products can take a picture of the top and sides of the container showing the best-by date and email the company for credit at: AR@wilcoxicecreamvt.com. Include quantity, place of purchase, name, address and telephone number. Wilcox Ice Cream can be reached at (802) 375-1133 Monday through Friday from 8:30 a.m. to 5 p.m. Eastern time.

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  • ZLINE expands recall of potentially deadly gas stoves to include replacement or refund option

    ZLINE expands recall of potentially deadly gas stoves to include replacement or refund option

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    ZLINE is expanding a recall of 30,000 gas ranges to provide consumers the option of a replacement range or refund.

    Recalled in January, the gas stoves may emit dangerous levels of carbon monoxide — a colorless, odorless gas — when in use, putting consumers at risk of serious injury or death from carbon monoxide poisoning, according to a notice posted by the U.S. Consumer Product Safety Commission.

    Common symptoms of carbon monoxide poisoning include headache, dizziness, weakness, upset stomach, vomiting, chest pain, and confusion. Breathing in high levels of carbon monoxide can cause you to pass out and may be fatal. 

    ZLINE, a family-owned company based in the U.S., issued this latest recall expansion after attempts to repair the gas ranges proved unsuccessful.

    “After the recall was announced, ZLINE received 131 reports that the repair was not completed successfully and that the ranges were still emitting dangerous levels of carbon monoxide,” the CPSC notice stated.

    Manufactured in China, the recalled ranges were sold in three sizes: 30 inches, 36 inches and 48 inches, the recall notice shows. Consumers can identify their unit’s model number by checking a label on the back of the gas range, according to the manufacturer. 

    Consumers of affected ranges should immediately stop use of the gas oven compartment and contact the manufacturer for a free inspection, replacement range or refund, the CPSC said.  

    The recall covers roughly 30,000 gas ranges sold online and in person at stores nationwide, including Best Buy, Lowe’s, The Home Depot and The Range Hood Store. The appliances were sold from February 2019 to December 2022 for between $2,300 and $6,900, according to the CPSC’s notice, and include the following model numbers:

    -RG48
    -RGS-48
    -RGB-48
    -RG30
    -RGS-30
    -RGB-30
    -RG36
    -RGS-36
    -RGB-36

    Customers with questions can call ZLINE toll-free at 833-226-1400 from 9 a.m. to 8:30 p.m. ET Monday through Friday, or send an email to rgrecall@zlinekitchen.com. They can also visit the manufacturer’s website at www.zlinekitchen.com/recalls or www.zlinekitchen.com and click on the banner at the top of the page for more information.

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  • Nationwide recall of peaches, plums and nectarines linked to deadly listeria outbreak

    Nationwide recall of peaches, plums and nectarines linked to deadly listeria outbreak

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    Peaches, plums and nectarines distributed by HMC Farms and sold nationwide as recently as last week are being recalled due to an outbreak of listeria that has resulted in 11 illnesses, including one death and 10 hospitalizations, federal safety regulators said Monday.

    “Investigators are working to determine if any additional fruit or products made with this fruit may be contaminated,” the U.S. Centers for Disease Control and Prevention stated in a food safety alert

    Kingsburg, California-based HMC Farms is recalling peaches, plums and nectarines sold between May 1 and November 15 of this year as well as as during the same period in 2022, the company said in a notice posted Friday by the Food and Drug Administration. The FDA found listeria in testing a sample of HMC Farms peaches in late October, the CDC said.

    Sold around the U.S. by retailers including Walmart and Sam’s Clubs, the recalled fruit may be contaminated with listeria monocytogenes, an organism that can cause serious and at times fatal infections. 

    As of Nov. 17, the people sickened in the listeria outbreak reside in seven states: California, Colorado, Florida, Illinois, Kansas, Michigan and Ohio, according to the CDC. One person died in California and another became sick while pregnant and had preterm labor, the agency noted.

    Listeria infections can cause serious, and sometimes fatal, illness in young children, frail or elderly people, as well as others with weakened immune systems, according to the CDC. Healthy people may experience symptoms including high fever, severe headache and stomach pain. The organism can also cause miscarriages and stillbirths.

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    Image of fruit recalled by HMC Farms due to listeria concerns.

    U.S. Food and Drug Administration


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    U.S. Food and Drug Administration


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    Image of recalled product.

    U.S. Food and Drug Administration


    The recalled fruit was sold in 2-pound bags branded “HMC Farms” or “Signature Farms,” or as individual fruit that has a “USA-E-U” code and a number, as follows:

    • Yellow peach: 4044 or 4038
    • White peach: 4401
    • Yellow nectarine: 4036 or 4378
    • White nectarine: 3035
    • Red plum: 4042
    • Black plum: 4040

    The recall does not include organically grown fruit, the company and CDC noted (See images of all of the recalled fruit products here).

    Consumers should check their homes, including their freezers, for the recalled fruit and discard it, agency said. Anyone with questions can call the company at (844) 483-3867, Monday-Friday from 8 a.m. to 8 p.m. Eastern time.

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  • Experts provide tips on how to avoid getting sick from your food

    Experts provide tips on how to avoid getting sick from your food

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    A listeria outbreak linked to peaches, plums and nectarines has sickened 11 people in seven states, and one person has died, according to the Centers for Disease Control and Prevention. The CDC estimates there are 48 million cases of foodborne illness in the U.S. every year. 

     For Meghan Elarde, a case of food poisoning turned her into a cautious shopper. 

    “I got so violently ill. It was frightening,” she told CBS News. 

    She said the experience caused her to become “way more concerned” about her groceries. Now, she buys hydroponic lettuce — leaves that are grown in water instead of soil — from Tom’s Market in Warrenville, Illinois.

    “I buy it because it is grown in a controlled environment,” she said. “I like it. There’s no pesticides added. There’s not a million people touching it and messing with it.”

    Elarde used to buy bagged lettuce, which, along with other leafy greens, is number one on Consumer Reports’ 10 Risky Recalled Foods list due to the number of illnesses, outbreaks and recalls they’ve been linked to.

    “Bagged lettuce has been through a lot of steps before it gets to you,” Sana Mujahid, a food microbiologist and Consumer Reports’ director of food safety, told CBS News. “It’s grown in a field. It’s taken through a processing plant. It’s cut up. It’s bagged. So, there are a lot of chances for contamination.”

    The same applies to pre-cut fruit, so Mujahid recommends buying whole fruit and cutting it yourself.

    Cheese and deli meats, ground beef, onions, turkey, chicken, papaya, peaches, melon and flour also made it onto Consumer Reports’ list of risky foods.

    If a melon’s rind comes in contact with contaminated irrigation water, when cut it can transfer to the fruit. Experts say to avoid bruised onions and produce because bacteria can enter and cause gastrointestinal issues, which can be serious for the immunocompromised.

    More than 3,000 die from foodborne illness every year, according to the CDC.

    Experts say it’s also important to be aware of recalls and to prepare your food with care.

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  • Which eye drops have been recalled? Full list of impacted products from multiple rounds of recalls.

    Which eye drops have been recalled? Full list of impacted products from multiple rounds of recalls.

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    FDA warns against using 26 eye drop products due to infection risk


    FDA warns against using 26 eye drop products due to infection risk

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    The FDA has expanded its list of eye drops recalled in 2023 because the products could be tainted with bacteria.

    Store-brand products sold at retailers including CVS, Rite Aid, Target and Walmart are included in the latest recall, posted on Wednesday by the federal safety agency. The recall by Kilitch Healthcare India cited “safety concerns” after FDA investigators found unsanitary conditions at the facility where the products were made.

    The FDA has cited a “risk of eye infections that could result in partial vision loss or blindness” in cautioning consumers against using the now-recalled products in late October. FDA investigators found bacteria in samples taken from the production plant, the agency noted in its warning. As of Nov. 13, Kilitch said it hasn’t received any reports of adverse health effects linked to the recall.

    Eye drops recalled in most recent round

    Many of the eye drops are likely no longer in stores, as the FDA said CVS, Rite Aid and Target were removing the products from store shelves and websites.

    The recall notice urged distributors and retailers to stop selling the products and for consumers to return them.

    Amazon removes 7 eye drop products from site after FDA warning

    Amazon said its website was no longer offering seven eye drop products after the FDA warned the e-commerce giant that their distribution violated federal regulations and raised public health concerns. 

    The pulled products named in the agency’s letter are: Similasan Pink Eye Relief, The Goodbye Company Pink Eye, Can-C Eye Drops, Optique 1 Eye Drops, OcluMed Eye Drops, TRP Natural Eyes Floaters Relief and Manzanilla Sophia Chamomile Herbal Eye Drops.  

    “We require all products offered in our store to comply with applicable laws and regulations. The products in question have been investigated and removed,” an Amazon spokesperson told CBS MoneyWatch on Friday in an emailed statement.

    Eye drops recalled in previous rounds

    The FDA’s warning prompted Cardinal Health in early November to recall six Leader brand eye products, while Harvard Drug Group recalled Rugby Laboratories brand eye drops. 

    Those warnings included the agency in August advising people not to buy “Dr. Berne’s MSM Drops 5% Solution” and “LightEyez MSM Eye Drops – Eye Repair,” saying they presented serious health risks, including vision- and life-threatening infections. 

    The recalls are among eight such actions involving the FDA and eye drops this year, starting with news in early February that the Centers for Disease Control and Prevention (CDC) was investigating a cluster of infections related to artificial tears. 

    Federal inspectors found dozens of problems at Indian manufacturer Global Pharma Healthcare amid the multistate outbreak of rare and extensively drug-resistant bacteria linked by eye drops made by the company, which were branded as EzriCare and Delsam Pharma.

    The CDC ultimately identified 81 patients in 18 states. Of that that number, four people died, 14 reported vision loss and another four had to have their eyeballs surgically removed, the agency said in its last update in May. 

    How can I make sure my eye drops are safe?

    Eye drops must be sterile to be safe, and therefore need “much finer oversight on the manufacturing side” to ensure the products aren’t contaminated, Carri Chan, a business professor at Columbia University, recently told CBS MoneyWatch.

    The FDA maintains an updated list of eye drop products that people should get rid of. Users can also consult an eye drop manufacturer’s website to check if a product has been recalled. 

    Dr. Christopher Starr, a spokesperson for the American Academy of Ophthalmology, said people should seek medical help immediately if they have adverse reactions to eye drops, such as discharge, redness or pain, which can indicate an infection. People should also check a product’s expiration date before use.

    Consumers with questions about the recall can contact Kilitch at regulatory@kilitchhealthcare.com or Velocity Pharma, Kilitch’s distributor, at regulatory@velocitypharma.com. Eye drop users who experience adverse reactions can file a report with the FDA online or by downloading and mailing a pre-addressed form.

    —Elizabeth Napolitano contributed to this report.

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  • Another eye drop recall pulls 27 products off of CVS, Rite Aid, Target and Walmart shelves after FDA warning

    Another eye drop recall pulls 27 products off of CVS, Rite Aid, Target and Walmart shelves after FDA warning

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    FDA warns against using 26 eye drop products due to infection risk


    FDA warns against using 26 eye drop products due to infection risk

    00:33

    Another eye drop recall is pulling 27 products from store shelves, including store-brand products sold at retailers such as CVS, Rite Aid, Target and Walmart, with the recall coming about three weeks after the U.S. Food and Drug Administration warned people not to buy or use the eye drops.

    Kilitch Healthcare India is recalling eye drops with expiration dates ranging from November 2023 to September 2025, citing “safety concerns” due to FDA investigators finding unsanitary conditions at the facility where the products were made, according to a news release posted Wednesday by the agency. You can see the full list of recalled eye drops here.

    The FDA cited a “risk of eye infections that could result in partial vision loss or blindness” in urging against use of the products in late October, with the agency saying its investigators found unsanitary conditions and “positive bacterial test results” from areas of an unidentified manufacturing facility. As of Nov. 13, Kilitch said it hasn’t received any reports of adverse health effects linked to the recall.

    Some of the eye drops may have already been removed from stores, as earlier this month the FDA said CVS, Rite Aid and Target were taking the products off their shelves and websites. 

    The recall notice said that distributors and retailers that have any of the recalled products should stop distributing them. Consumers, meanwhile, should stop using the recalled eye drops and return the products to where they purchased them, the FDA said.

    Unsanitary conditions

    Bloomberg News reported that Kilitch produced the eye drops in an unsanitary factory in India where some workers went barefoot and others made up test results that purported to show the products were sterile. 

    The FDA’s warning prompted Cardinal Health in early November to recall six Leader brand eye products, while Harvard Drug Group recalled Rugby Laboratories brand eye drops. 

    The FDA earlier this year announced a spate of recalls of eye drop products linked to four deaths and multiple cases of vision loss. In August, it warned against using two additional eye drop products because of the risk of bacterial or fungal contamination. 

    Eye drop products, which must be sterile in order to be safe, require “much finer oversight on the manufacturing side in order to ensure that there’s no contamination whatsoever,” Carri Chan, a business professor at Columbia University, told CBS MoneyWatch last week in reference to the spate of recalls.  


    Good Question: What guidelines should we follow when buying eye drops?

    02:25

    The FDA keeps an updated list of eye drop products that consumers should discard. Users can also consult an eye drop manufacturer’s website to check if a product has been recalled. 

    Dr. Christopher Starr, a spokesman for the American Academy of Ophthalmology, said people should seek medical help immediately if they experience adverse reactions to their eye drops, told CBS MoneyWatch. Signs of an infection typically include discharge, redness or pain. Consumers should also check a product’s expiration date before use.

    Consumers with questions about the recall can contact Kilitch at regulatory@kilitchhealthcare.com or Velocity Pharma, Kilitch’s distributor, at regulatory@velocitypharma.com. Eye drop users who experience adverse reactions can file a report with the FDA online or by downloading and mailing a pre-addressed form.

    —Elizabeth Napolitano contributed to this report.

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