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
Herold Salads, Inc. recalls Amish Wedding Southern Potato Salad with egg due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.
Herold Salads, Inc. is recalling Amish Wedding Rotini Garden Medley due to potential Listeria monocytogenes contamination. The product was distributed in Ohio, Pennsylvania, and Michigan.
NBRBDR Inc. is recalling Zucchini Mushroom Pie (5 oz) due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.
Herold Salads, Inc. is recalling Herold's Macaroni Salad in 1lb to 10lb tubs due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.
Nutritious Delicious Foods is recalling assorted 2 oz pies distributed in California for undeclared egg, milk, and wheat allergens.
Cleveland's Own Macaroni Salad sold in 5-pound and 10-pound containers is being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.
Herold's Salads Southern Potato Salad with egg is being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.
Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.
TreeHouse Foods is recalling Organic Low/Reduced Sodium Chicken Broth sold under multiple brands due to potential microbial contamination. The recall affects 439,240 cases distributed across 37 states.
Smiths Medical is recalling High Pressure Rotators due to a manufacturing defect affecting O-ring seals. An oversized inner diameter may cause inadequate seal integrity, risking medication under-infusion.
Procter & Gamble is recalling Secret OUTLAST Dry Spray antiperspirant (3.8 oz) due to potential benzene contamination at the manufacturing facility. All lots expiring through September 2023 are affected.
Old Spice SWEAT DEFENSE Dry Spray anti-perspirant is being recalled due to manufacturing facility issues where other product lots were found contaminated with benzene. No illnesses have been reported.
Sarnova HC is recalling the Curaplex Field Cric Kit due to an incompatible endotracheal tube holder that prevents practitioners from securing the tube during cricothyrotomy procedures. The recall affects 1,063 kits distributed nationwide.
The CareEvent patient monitoring device may fail to send push notifications, potentially delaying detection of patient condition changes.
Oakworks Inc is recalling 28 Ultrasound EA examination tables due to backrest platform stress fractures that prevent operation in an inclined position.
Oakworks Inc is recalling 212 Ultrasound EA G2 examination tables nationwide due to stress fractures in the backrest platform that make the equipment non-operational in an inclined position.
Procter & Gamble is recalling Secret OUTLAST Dry Spray Antiperspirant due to a manufacturing facility deviation where other lots were found contaminated with benzene. The recalled product was manufactured at the affected facility.
Maquet Cardiovascular is recalling 38,094 units of the Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500, due to polyimide particulate matter contamination that may be introduced into the arterial conduit during coronary artery bypass or peripheral bypass surgery.
Getinge is recalling Maquet Volista OR light systems that may fall during use in operating rooms. Approximately 236,793 units are affected nationwide and globally.
Randox Calibration Serum Level 3 has an incorrect Alkaline Phosphatase target value (approximately 10% off) affecting clinical chemistry testing on RX Series instruments.
A surgical guide used in knee replacement is recalled due to mislabeling showing incorrect dimensions. This could result in improper bone resection and implant fit, potentially extending surgery time.
Philips Patient Information Center iX devices may fail to send push notifications under certain conditions, potentially delaying detection of patient condition changes. A total of 814 units have been recalled worldwide.
Smiths Medical is recalling 31,685 HIGH PRESSURE ROTATOR infusion devices with a manufacturing defect that may cause an inadequate seal. The defect could lead to medication leaks and under-infusion.
Smiths Medical is recalling Medex injection line rotating adapters due to a manufacturing defect where the O-ring inner diameter may be oversized, potentially causing medication leaks during infusion.
Walgreens Dye-Free Magnesium Citrate Saline Laxative is being recalled nationwide due to bacterial contamination. The FDA identified Acetobacter nitrogenifigens in the product.