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
TETAS Mireya, SABOR Galleta Oreo cookies are being recalled due to undeclared soy and wheat allergens. Consumers with soy or wheat allergies should not consume this product.
Environmental debris accumulation may block flow sensors in Philips ventilators, potentially preventing accurate pressure and flow delivery to patients.
Tastykake Chocolate Kandy Kakes are being recalled due to undeclared peanuts. The product poses a serious risk to individuals with peanut allergies.
BearCare's Walnut Wearable Smart Thermometer (Model WT20) is being recalled due to reports of skin burns in children ages 0-6. The device was distributed nationwide; 1818 units were affected.
Philips Respironics recalled approximately 57,395 ventilators due to environmental debris potentially accumulating on the flow sensor, which may prevent accurate delivery of pressure and volume to patients, risking hypoxemia.
DIBE LLC is recalling TETAS Mireya candy due to undeclared soy and walnut allergens. Consumers with allergies to these ingredients should not consume the product.
Olam Food Ingredients is recalling Onion Powder Premium sold in bulk fiber bags due to potential Salmonella contamination. Affected product was distributed to Canada, Arkansas, and Illinois.
DIBE LLC is recalling TETAS Mireya SABOR Galleta Maria cookies due to undeclared soy and wheat allergens. Consumers with allergies to these ingredients should not consume the product.
A software anomaly in StealthStation Cranial Software causes depth gauge displays to lose synchronization during cranial biopsy procedures, risking inaccurate surgical guidance and tissue injury.
Philips Respironics recalled 18,855 Trilogy Evo O2 EV300 devices because environmental debris may accumulate on the flow sensor, potentially causing inaccurate delivery of pressure or flow. This could result in patient hypoxemia if not promptly addressed.
Great Dane is recalling 2024 Champion and Everest trailers because tire pressure may drop at speeds over 45 mph, increasing crash risk.
Meijer Inc is recalling Frederik's by Meijer Dark Chocolate Almonds due to undeclared milk. The product was distributed to Meijer stores in six Midwest states.
Gonnella Frozen Products is recalling 949 cases of frozen brat roll dough due to undeclared egg. Egg was not disclosed on the product label.
Stoughton Trailers is recalling 2023-2024 Intermodal container chassis because improperly tightened wheel lug nuts can allow the wheel to detach, increasing crash risk.
The FDA has issued a Class I recall for the Trilogy Evo Universal Ventilator Model DS2000X11B, affecting 22,237 units distributed nationwide and globally. The device is manufactured by Philips Respironics, Inc.
Meijer Inc is recalling Meijer Express Dark Chocolate Covered Almonds due to undeclared milk, a serious risk for consumers with milk allergies. The recall affects 9,030 units in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
Golden State Medical Supply is recalling Travoprost eye drops due to missing tamper evidence seals on some bottles. The missing seal prevents sterility assurance on 1,920 units distributed nationwide.
Avanos Medical is recalling SMMT ambIT Reusable cassettes (Product Code 220568, Lot 30191805) that were potentially distributed without a required air-in-line filter. The missing component affects units in Texas, Oregon, and Australia.
BioReference Health is recalling the 4Kscore Test system due to software anomalies in its processing module that may generate erroneous diagnostic results. The recall affects 662 patient test results distributed in New Jersey.
Qiagen Sciences LLC recalls 347 QIAstat-Dx Respiratory SARS-CoV-2 test kits due to faulty cartridges that could produce false results. Affected kits were distributed nationwide in nine states.
Elekta, Inc. is recalling 18 Elekta Unity Image-Guided Radiation Therapy Systems due to a potential electrical connector overheat hazard in the MR gradient coil. No injuries have been reported.
Avanos Medical recalls some AVNS ambIT System catheter kits that were potentially distributed without an air in-line filter. Affected units were distributed worldwide, including in Texas, Oregon, and Australia.
DIBE LLC is recalling TETAS Mireya, SABOR Toddy products that may contain undeclared soy allergen. Consumers with soy allergies should not consume this product.
DePuy Mitek BIOKNOTLESS Rapid surgical anchor inserters may fracture during use, potentially retaining fragments in patients. Removal during surgery may cause bone damage and extended surgical time.
C.R. Bard is recalling Magic3 Go Intermittent Urinary Catheters because the clear resealing label can separate from the pouch, potentially compromising sterility. The recall affects devices distributed worldwide.