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
Dr. Praeger's Sensible Foods Inc. is recalling Simply Nature Spinach Bites (12 oz) due to the possibility of rodent hair contamination. The affected product was distributed to Maryland and Pennsylvania.
Apotex Corp. is recalling brimonidine tartrate/timolol maleate ophthalmic solution nationwide due to lack of sterility assurance. The recall affects 107,136 vials across two lots.
Strides Pharma is recalling Children's Ibuprofen Oral Suspension due to the presence of gel-like masses and black particles found in the product. Affected lots 7261973A and 7261974A should not be used.
Somerset Therapeutics LLC recalled 62,190 vials of Dexamethasone Sodium Phosphate Injection due to out-of-specification impurities detected during stability testing. The affected lot was found to contain elevated levels of certain degradation products at product expiry.
Howmedica Osteonics' MICS3 Angled Sagittal Saw Attachment screws may loosen and detach during use. The recall affects approximately 1,098 units distributed nationwide and internationally.
Elekta recalls Leksell Gamma Knife radiosurgery systems where the adapter may not be properly aligned or locked in place, potentially affecting treatment delivery accuracy.
ConvaTec EsteemBody Drainable Pouches may leak due to a manufacturing defect. The affected products (Ref 423643, 10-45mm, UDI 00768455221264, lots 5K00011 and 5K00714) are distributed worldwide.
Stryker is recalling Cub Pediatric Cribs (Model FL19H) due to missing access door warning labels that could affect proper equipment use.
Centricity Universal Viewer Software has a cybersecurity vulnerability that may expose user login credentials on workstations. Unauthorized individuals could impact system availability or manipulate medical data.
The Welch Allyn Spot Vision Screener VS100 may display flickering due to a software issue. Flickering light exposure could trigger photosensitive seizures in susceptible individuals.
Wagner Spray Tech recalled about 700,000 power steamers because the hose and nozzle can get excessively hot, causing burns. Over 50 consumers reported burn injuries, many first- or second-degree.
Electrolux is recalling about 174,800 Frigidaire gas ranges for a delayed oven ignition hazard that has caused 30 reported burn injuries. Free repairs are available.
Tainoki Fine Furniture is recalling about 2,200 swivel office chairs sold at HomeGoods because the chair base can bend and cause a fall hazard. No injuries have been reported.
Goregent infant walkers sold on Amazon are recalled because they can fit through standard doorways and fail to stop at stairs, creating a fall hazard. No injuries have been reported.
BUILT LUUM light-up tumblers can break, exposing button cell batteries that pose choking and ingestion hazards to children. Approximately 75,700 units were sold from October 2024 through December 2025.
Specialized Turbo Como SL electric bicycles' fork steerer tubes can develop fatigue cracks leading to failure and fall risk. About 5,720 units sold March 2021–January 2026 are affected.
Approximately 200 Aisstxoer adult bicycle helmets sold on Amazon violate mandatory safety standards and may fail to protect against head injury. Consumers should stop using them immediately and contact the seller for a refund.
Amazon is recalling about 2,840 Camping Folding Pocket Knives because the blade's folding mechanism can fail to stay closed, posing a laceration hazard. No injuries have been reported.
Made Fresh Salads brand Sundried Tomato Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact the manufacturer or their retailer.
Made Fresh Salads brand Jalapeno Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. All products with expiration dates through February 27, 2026 sold in New York are affected.
Made Fresh Salads brand Walnut Raisin Cream Cheese in 5 lb tubs is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects products distributed in New York with expiration dates through 2/27/2026.
Made Fresh Salads brand Tofu Whipped in 5 lb tubs is being recalled because products may be contaminated with Listeria monocytogenes. The recalled product was distributed in New York.
Trividia Health is recalling instructions for TRUE METRIX blood glucose meters because E-5 error code guidance is inadequate, potentially delaying treatment for dangerously high blood sugar levels.
Made Fresh Salads brand Caramel Apple Cream Cheese in 5 lb tubs is being recalled because it may be contaminated with Listeria monocytogenes. The recall affects product distributed in New York with expiration dates through February 27, 2026.
Made Fresh Salads brand Whipped Cream Cheese in 5 lb tubs is being recalled due to potential contamination with Listeria monocytogenes. The product was distributed in New York.