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Fda Recall

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FDA Expands Jalapeño Recall Across Major Retailers in 26 States
us14 days ago

FDA Expands Jalapeño Recall Across Major Retailers in 26 States

The FDA has broadened a recall of jalapeño-containing foods distributed to Hannaford, Kroger, Stop & Shop, Target, Trader Joe’s, Walmart, Whole Foods, and other retailers in 26 states due to a Salmonella Javiana outbreak linked to Coast Citrus jalapeños; Taylor Farms issued its own jalapeño-related recall after sourcing from Coast Citrus, and no illnesses tied to the Taylor Farms jalapeño products have been reported yet. The recalled items span dips, salsas, pico de gallo, burritos, and various store-brand products. Consumers who purchased affected items should discard them and request refunds from retailers or contact Taylor Farms for questions; the FDA and CDC continue investigating the multi-state outbreak.

via Yahoo News Canada|
#coast-citrus-distributors#fda-recall#jalapeno-peppers
Nationwide Recall: Subpotent Levothyroxine Pills Prompt FDA Action
health29 days ago

Nationwide Recall: Subpotent Levothyroxine Pills Prompt FDA Action

The FDA issued a Class II recall for certain levothyroxine sodium tablets used to treat hypothyroidism after tests found subpotent levels of the active ingredient, potentially reducing effectiveness. Major Pharmaceuticals and Cardinal Health distributed twelve recalled dosages nationwide in cartons; the recall covered multiple lots, but the total quantity was not disclosed.

via NBC 7 San Diego|
#class-ii-recall#fda-recall#health
FDA flags false-positive cyclosporiasis result, reshaping outbreak link to iceberg lettuce
health1 month ago

FDA flags false-positive cyclosporiasis result, reshaping outbreak link to iceberg lettuce

Delaware reports its first cyclosporiasis case this year as part of a multistate outbreak still under investigation; nationwide cases exceed 1,600 with 94 hospitalizations, though many infections go unreported. The FDA has concluded a recent cyclospora lab signal was a false positive, removing the previously suspected link to iceberg lettuce tied to Taco Bell. The Taylor Farms de Mexico iceberg lettuce recall remains in effect and Walmart-distributed products are among those affected; the public is advised to discard recalled lettuce and clean affected surfaces while investigators continue to determine the true source.

via Delawareonline.com|
#cyclosporiasis#false-positive#fda-recall
RFK Jr: Cyclospora outbreak under control after FDA flips lettuce recall decision
health1 month ago

RFK Jr: Cyclospora outbreak under control after FDA flips lettuce recall decision

US health secretary Robert F Kennedy Jr. says the cyclospora outbreak is under control after the FDA reversed a 27-state shredded iceberg lettuce recall as a false positive. CDC data show 34 states affected with over 1,600 confirmed and about 5,100 pending cases, with Michigan heavily hit. The administration’s forensics identified a likely source and the involved companies implemented recalls, while critics note CDC response delays linked to prior budget and staff cuts to public health programs and surveillance.

via The Guardian|
#cyclospora#fda-recall#health
FDA recalls about 244,432 carbamide peroxide ear drops nationwide for subpotent ingredient
science1 month ago

FDA recalls about 244,432 carbamide peroxide ear drops nationwide for subpotent ingredient

The FDA is recalling about 244,432 containers of 6.5% carbamide peroxide earwax-removal products distributed nationwide due to subpotent active ingredient, potentially yielding ineffective results. The recall, classified as Class II, covers multiple brands (including CVS Health, Clinere, QC Quality Choice, TopCare Health, Audiologist's Choice, Family Wellness, Good Neighbor Pharmacy, Leader, Foster & Thrive, Meijer, CAREone) and advises consumers not to use these lots until replacement or further guidance is issued.

via Yahoo|
#carbamide-peroxide#class-ii-recall#earwax-removal
FDA Elevates Utz Chip Recall to Class 1 Over Salmonella Risk
health1 month ago

FDA Elevates Utz Chip Recall to Class 1 Over Salmonella Risk

The FDA has designated Utz’s recall of certain Dirty and Zapp’s potato chips as Class 1—the most serious level—due to potential salmonella from dry milk powder used in seasoning. The recall covers multiple sizes and flavors totaling over 650,000 bags; Utz has said no illnesses have been reported. Consumers who bought recalled products should discard them and can seek refunds by contacting Utz.

via NBC News|
#dirty-brand#fda-recall#health
FDA Class I Recall Hits Zapp's and Dirty Brand Potato Chips Over Salmonella Risk
health1 month ago

FDA Class I Recall Hits Zapp's and Dirty Brand Potato Chips Over Salmonella Risk

The FDA classified Utz Quality Foods’ recall of Zapp's and Dirty-brand potato chips as Class I, its highest risk level, due to potential salmonella contamination from a dry milk powder used in seasoning. More than 650,000 bags sold across the United States were recalled. Consumers should not eat the affected chips and should discard them, checking best-by dates and batch codes; refunds are available from Utz Customer Care.

via Yahoo|
#fda-recall#health#potato-chips
FDA Recalls Magnesium Glycinate Gummies Over Undeclared Melatonin
science2 months ago

FDA Recalls Magnesium Glycinate Gummies Over Undeclared Melatonin

The FDA issued a Class II recall for 13,920 bottles of Adndale magnesium glycinate gummies manufactured by Dkiru LLC (Dublin, Ireland) due to undeclared melatonin, with recalls announced June 19 (starting May 12) and tied to LOTs 190824, 240923, and 240929 (EXP 08/19/2026, 09/22/2026, 09/28/2026). The Cleveland Clinic notes excessive magnesium can cause GI symptoms, low blood pressure and other issues, with general daily allowances around 400 mg for men and 320 mg for women. Consumers should check the UPC 86000878455111 and the recalled lots, and dispose/return if affected.

via Yahoo|
#cleveland-clinic#fda-recall#magnesium-glycinate
Nationwide recall: Spring & Mulberry chocolates flagged for salmonella risk
food-safety3 months ago

Nationwide recall: Spring & Mulberry chocolates flagged for salmonella risk

The FDA issued a nationwide recall of Spring & Mulberry chocolate bars after confirming an ingredient contaminated with salmonella; affected flavors and batch codes are listed, and customers who bought these items should not consume them and should discard or return them for a refund due to potential serious illness, especially in young children, the elderly, or immunocompromised individuals.

via WKRC|
#chocolate#consumer-warning#fda-recall
FDA recalls oysters and clams over possible norovirus contamination across nine states
food-and-drink5 months ago

FDA recalls oysters and clams over possible norovirus contamination across nine states

Federal officials announced a recall of raw oysters from Drayton Harbor Oyster Company and Manila clams from Lummi Indian Business Council sold in at least nine states due to potential norovirus contamination. Oysters were distributed to consumers in Washington, while clams were sent to restaurants and retailers in Arizona, California, Florida, Georgia, Illinois, Nevada, New York, Oregon and Washington. The FDA warns norovirus can look and taste normal but cause illness, with symptoms like diarrhea and vomiting; high-risk individuals should avoid consumption. Harvest dates were February 13–March 3 in Drayton Harbor, Washington.

via CBS News|
#clams#fda-recall#food-and-drink
Blue-plastic contamination prompts nationwide peanut butter recall
health6 months ago

Blue-plastic contamination prompts nationwide peanut butter recall

The FDA issued a recall for three Ventura Foods-produced peanut butter products after detecting blue plastic foreign material, affecting jars sold across 40 states. The recall was reclassified to Class II on Feb 12, 2026. There is no FDA-mandated remedy, but customers can obtain refunds by returning recalled jars to the place of purchase; a full list of affected items is in the recall report.

via WKRC|
#class-ii-recall#fda-recall#foreign-material
FDA raises pecorino romano cheese recall to highest risk level amid listeria findings
health7 months ago

FDA raises pecorino romano cheese recall to highest risk level amid listeria findings

The FDA has upgraded a nationwide pecorino romano cheese recall to Class I, indicating a reasonable probability that exposure could cause serious health consequences or death, after listeria monocytogenes was detected. The recall, originally issued Nov. 25, 2025 by Ambriola Company, covers eight products across brands such as Locatelli, Pinna, Boar’s Head, Member’s Mark (Sam’s Club), and Ambriola Picante in various sizes and packaging, distributed to 20 states. Consumers should discard the recalled cheese or return it for a refund; there have been no reported illnesses.

via Yahoo|
#cheese-recall#class-i-recall#fda-recall
FDA Recalls Popular Blood-Pressure Medication
health7 months ago

FDA Recalls Popular Blood-Pressure Medication

The FDA has issued a low-risk recall for over 11,000 bottles of Ziac, a blood-pressure medication, due to cross-contamination concerns with ezetimibe. Patients should check their bottles' lot numbers and NDC codes, and consult their healthcare providers for guidance. The recall highlights the importance of strict manufacturing practices and vigilant quality control to ensure medication safety.

via Earth.com|
#blood-pressure-medication#cross-contamination#drug-safety