Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Giant Eagle's Brownie Tray Classic brownies made with Jiff Peanut Butter are being recalled due to potential Salmonella contamination. The product was distributed in Pennsylvania.
Giant Eagle brand mini chocolate gobs with peanut butter icing are being recalled due to potential Salmonella contamination from Jiff peanut butter used in manufacturing. The product was distributed in Pennsylvania.
Palindrome H Chronic Catheters are being recalled due to a potential leaking condition in the catheter hub that may result in unanticipated fluid return during hemodialysis treatment. Affected units have been distributed worldwide.
Covidien is recalling Palindrome Chronic Catheters due to a potential leaking condition in the hub that may cause unexpected fluid return during use.
The 2022 Toyota Tundra with Panoramic View Monitor may display front camera footage instead of rear camera when in reverse, reducing rear visibility and increasing crash risk. Toyota will reprogram the parking assist system free of charge.
Giant Eagle's Peanut Butter Fudge Split Cake, made with Jiff Peanut Butter, is being recalled due to potential Salmonella contamination. The recall affects units distributed in Pennsylvania.
Covidien is recalling certain Palindrome Precision H Chronic Catheters because the hub may leak, causing unexpected fluid to flow back during use. This FDA Class I recall affects 26,675 units distributed globally.
Covidien is recalling Mahurkar Chronic Carbothane dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use. Approximately 132,443 units distributed worldwide are affected.
Giant Eagle is recalling a 16-ounce Peanut Butter Creme Brownie made with Jiff Peanut Butter due to potential Salmonella contamination. The product was distributed to Pennsylvania.
Pure Ground Ingredients has recalled specific lots of organic oregano leaf powder and ground oregano sold in Oregon, Wisconsin, Maryland, and Colorado due to potential Salmonella contamination.
Giant Eagle Torte Peanut Butter (62 oz, code GE 23984200000) is recalled due to potential Salmonella contamination from the Jiff peanut butter ingredient. Consumers should not consume this product.
Giant Eagle Petite Cake Peanut Butter 18Oz, distributed in Pennsylvania, is recalled due to potential Salmonella contamination. Products were manufactured using Jiff Peanut Butter.
Giant Eagle Brownie Classic Peanut Butter is recalled due to potential Salmonella contamination from the Jiff Peanut Butter ingredient. Affected product distributed in Pennsylvania.
Giant Eagle's GE Bakery peanut butter thumbprint cookies are recalled due to potential Salmonella contamination from Jiff peanut butter. The 12-ounce packages distributed in Pennsylvania should not be consumed.
Covidien recalls Palindrome Precision SI chronic dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use.
Siemens Dimension CTNI cardiac troponin test is recalled for positive bias (falsely elevated readings) in Lithium Heparin plasma samples, which may lead to misdiagnosis of myocardial infarction.
Chromsystems is recalling MassCheck Amino Acid Acylcarnitines dried blood spot control material due to too-low glycine concentration in batch 2821. The defect was found in units distributed to New York, Ohio, and Connecticut.
Fresenius Medical Care recalled NaturaLyte 2301 dialysate in Texas and Louisiana after exposure to below-recommended storage temperatures. The exposure may cause packaging leaks, potentially leading to biological contamination and bloodstream infection risk.
EAT REAL FOOD LLC is recalling Culina Plant Based Yogurt nationwide due to potential glass fragments in the product. Affected units were distributed to all states.
Ossur has recalled 410 Variflex Suba Junior prosthetic feet due to cracking and breaking under impact stress. The device is designed for children and adolescents worldwide.
EAT REAL FOOD LLC is recalling Culina Plant Based Blueberry Lavender Yogurt due to potential glass fragments. Affected lots were distributed nationwide with best-by dates in October and November 2022.
EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Mango Orange Blossom due to potential glass contamination. The affected lot code is 07422CBCUCYMOB0723 with best-by date 11/13/2022, distributed nationwide.
Paris Brothers Inc is recalling Mild Cheddar Cheese (UPC 033954252225) due to Listeria in environmental samples. The affected lots (05042022 and 05052022) were distributed to wholesalers, retailers, and food service establishments.
EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Bourbon Vanilla in 5 oz. glass jars nationwide due to potential glass fragments in the product. Consumers should not consume products with the affected lot codes.
Rayner is recalling RayOne intraocular lens injection systems because the outer package is mislabeled and contains a different lens strength than indicated. Approximately 162 devices were distributed in 13 US states.