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 deaths or serious injuries are reported, 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
Endliss Technology is recalling Trianium battery phone cases because the lithium-ion batteries can overheat and cause burns. Consumers should stop using them and contact the company for a replacement.
Spokane Produce, Inc. is recalling Epicurean Greek Salad Kits because they contain onion supplied from Thomson International, Inc., which is associated with Salmonella Newport.
Spokane Produce, Inc. is recalling 8-ounce containers of Fresh Medium Salsa because the product contains onion supplied by Thomson International, Inc., which is associated with Salmonella Newport.
Spokane Produce, Inc. is recalling refrigerated stew mix trays because they contain onion supplied from a source associated with Salmonella Newport.
Spokane Produce, Inc. is recalling unlabeled diced onions distributed in the Pacific Northwest and Mountain West due to a Salmonella Newport contamination risk.
Spokane Produce, Inc. is recalling refrigerated chicken salad sandwiches because they contain onion supplied by a source linked to Salmonella Newport.
CB2 is recalling Bordo and Bordo XL dining tables because the legs can become unsteady, causing the table to collapse and posing an injury hazard.
Spokane Produce, Inc. is recalling refrigerated potato salad containing onion supplied by Thomson International, Inc. due to a Salmonella Newport risk.
Riverpoint Medical is recalling 1,262 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Riverpoint Medical is recalling 1,256 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
ESAOTE is recalling AC/DC power adapters for specific portable ultrasound systems because the connector may heat up, smoke, or melt due to mechanical stress.
Philips North America, LLC is recalling 71 ProxiDiagnost N90 systems in the United States because an unexpected increase in peak tube potential may lead to increased patient radiation dose.
4e Brands North America is recalling blumen Clear Advanced Hand Sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor Current Good Manufacturing Practices.
Spokane Produce is recalling Trifecta Delight Salad Kits because they contain onion supplied by Thomson International, Inc., which is associated with Salmonella Newport.
FDA is recalling Endo GIA Auto Suture Universal Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
4e Brands North America is recalling Assured Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination, representing poor CGMP practices.
Riverpoint Medical is recalling 9,214 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
4e Brands North America is recalling Modesa hand sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor manufacturing practices.
4e Brands North America is recalling Blumen Advanced Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.
Direct Rx is recalling 33 bottles of Losartan Pot/HCTZ 50/12.5 mg tablets distributed in Florida due to trace amounts of impurity NMBA.
Eagle Family Foods Group LLC is recalling Nice! Organic White Cheddar Popcorn because pieces of glass may be present in the product.
Riverpoint Medical is recalling 1,253 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. This defect could compromise the sterile field and increase the risk of surgical site infection.
4e Brands North America is recalling Blumen Advanced Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.
4e Brands North America is recalling ASSURED Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination, representing poor CGMPs.
Riverpoint Medical is recalling 1,875 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.