A recall was just announced on approximately 180,100 ovens sold across the U.S. and Canada, according to the Consumer Product Safety Commission (CPSC).1 This is due to the ranges posing a burn hazard.
The oven ranges affected are Frigidaire, Frigidaire Gallery and Frigidaire Professional gas ranges with one of the following model numbers: Read More –
Strides Pharma, Inc. is recalling 89,592 bottles of ibuprofen distributed nationwide.
The product, Children’s Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, was manufactured for Taro Pharmaceuticals USA, Inc.
The recalled products have lot numbers 7261973A and 7261974A with an expiry date of Jan. 31, 2027. Read More –
Dr. Praeger’s is recalling Aldi-exclusive Simply Nature Spinach Bites after possible contamination with rodent hair, according to the FDA.The recall affects 7,894 units of 12-ounce boxes distributed only in Maryland and Pennsylvania, identified by lot number G25CF-02B and UPC 4099100247992.The FDA classified the recall as Class II, advising consumers not to eat the product and to discard it or return it for a refund. Read More –
The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen ready-to-eat turkey stuffed pastry products due to misbranding. Some boxes of the turkey, pesto, and cheese stuffed pastries contain ham and cheese instead. A recall was not requested because the product is no longer available for purchase.
| Cream Cheese Recalled by FDA for Possible Death, Marking Highest Warning Level People.com Numerous cream cheese products from Made Fresh Salads have been recalled by the Food and Drug Administration (FDA), as they have the potential to … |
| Multivitamin Recall Update for 25 States As FDA Sets Risk Level – Newsweek Newsweek FDA records show the recall affects 422 cases of the 0.25 mg product and 210 cases of the 1.0 mg product, with each case containing 12 bottles of 100 … |
| Herbal supplement recalled after FDA analysis finds undeclared active ingredient in Viagra abc7NY The FDA says that sildenafil was not listed on the supplement product label. The undeclared ingredient may interact with nitrates found in some … |
Costco has issued a recall for a ready-to-eat deli meal sold in 26 states, plus the District of Columbia and Puerto Rico, for potential Salmonella contamination. The prepared Meatloaf with Mashed Yukon Potatoes and Glaze, sold under Costco item number 30783, has been recalled after an ingredient in the meatloaf was found to be contaminated with the bacteria. Read More –
Lidl US Issues Allergy Alert on Undeclared Hazelnuts in Favorina Chocolate Ladybugs – German-Style Nougat
ARLINGTON, VA – Lidl US is recalling all lots of their Favorina Chocolate Ladybugs – German-Style Nougat 3.52 oz box UPC 20304492 due to undeclared hazelnut allergen. People who have allergies to hazelnuts run the risk of serious or life-threatening allergic reactions if they consume these products.
Pure Vitamins and Natural Supplements, LLC Issues Voluntary Nationwide Recall of Honey Products Due to Undeclared Sildenafil and Tadalafil
March 14, 2026- Pure Vitamins and Natural Supplements, LLC of Tampa, FL is voluntarily recalling Boner Bear Honey, Red Bull Extreme and Blue Bull Extreme. FDA laboratory analysis confirmed that Boner Bear Honey, contains sildenafil and tadalafil and Red Bull Extreme and Blue Bull Extreme contains sildenafil not listed on the product label.
An E. coli outbreak is being linked to Raw Farm-brand raw cheddar cheese products. Seven illnesses, including two hospitalizations, have been reported in three states. The FDA advises disposing of the cheddar cheese and sanitizing infected surfaces. Read More –
| Cream Cheese Recall Upgraded Over Listeria Risk, FDA Says – U.S. News & World Report U.S. News & World Report The U.S. Food and Drug Administration (FDA) said certain cream cheese products made by Made Fresh Salads Inc. may contain Listeria monocytogenes … |
Convenience Kit Needle Recall: Integra LifeSciences Removes Tuohy Needle | FDA
The FDA has since determined that this device may cause temporary or reversible health problems, or—though unlikely—serious health problems.
