(Please note – Many times you hear about a recall, but don’t see it here. Often I reported on it as soon as I received it. Check last week’s recall.)
011-2026, Maple Leaf Foods Inc. Recalls Not Ready-To-Eat (NRTE) Bacon Product Imported without the Benefit of Import Reinspection (Jul 24, 2026)
FSIS Issues Public Health Alert for Steak Burrito Product Due to Misbranding and Undeclared Allergen
The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for a Steak, Cilantro, Lime Burrito product due to misbranding and an undeclared allergen. The product contains egg, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to egg products are aware that this product should not be consumed.
529 Commerce LLC Recalls Rooted in Rare brand Aquafaba Powder due to Undeclared Eggs
529 Commerce, LLC of Parkland, Florida is recalling 3,860 units of its 4oz and 12 oz packages of its Rooted in Rare brand Aquafaba Powder because the product may contain undeclared egg.
FSIS Issues Public Health Alert for Curried Chicken Salad Product that May Be Contaminated with Listeria
Mary’s Harvest Fresh Foods, Inc. The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for Curry Chicken Salad due to concerns that the product may be contaminated with Listeria monocytogenes (Lm). A recall was not requested because the products are no longer available for purchase.
Evenflo has recalled certain REO by Revolve360 car seats because the headrest may shift during a crash, reducing safety.
Parents can check if their car seat is affected by locating the model number and manufacture date on the back of the headrest.
Evenflo is working on a free repair kit and will notify registered owners when it’s ready. Read More –
(NewsNation) — Major Pharmaceuticals is voluntarily recalling a popular thyroid medication, federal regulators announced this month.
The Levothyroxine Sodium Tablets were recalled because they are subpotent, meaning they are not fully effective, the Food and Drug Administration (FDA) said. The medication is used to treat hypothyroidism and goiter, among other conditions, according to the Mayo Clinic.
The recall was designated a Class II on July 17, meaning the tablets may cause temporary adverse health consequences, the FDA said. Read More –