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
Qiagen's therascreen FGFR RGQ RT-PCR Kit is being recalled for increased false positive results in 29 distributed kits. False positives could lead to incorrect lab reports and inappropriate cancer treatment for patients.
A software error in the Pentacam HR eye imaging device causes inaccurate IOL calculator output for toric intraocular lens surgical planning. Nineteen systems are affected.
Nissan is recalling 2020-2023 Titan vehicles and certain other models because the transmission parking pawl may fail to engage in park, risking vehicle rollaway and crash.
Honda is recalling 2020-2021 CRF1100 Africa Twin motorcycles due to an ECU software error that may cause engine stall or loss of drive power. Owners can get a free software update from dealers.
UPPAbaby is recalling about 14,400 All-Terrain RIDGE jogging strollers because openings in the rear disc brakes can catch and amputate a child's fingertip. One injury has been reported.
Entegra and Jayco motorhomes may have incorrectly installed torsion bar shims causing potential suspension failure. Dealers will replace the defective component free of charge.
Jayco is recalling 2021-2023 Entegra and Jayco motorhomes for a missing water drain in the engine air intake box. Water can accumulate and enter the engine, causing engine failure and increasing crash risk.
Nissan is recalling certain 2021-2022 Rogue vehicles where rear seat belts may not retract properly, making them difficult to use. This could prevent proper seatbelt usage in a crash. Dealers will replace affected seat belts for free.
TJX Companies is recalling about 5,000 Novogratz outdoor metal hanging chairs sold nationwide. These chairs can tip or fall while occupied, or the supporting hooks or chains can break, causing 16 reported injuries including bruises and a mild concussion.
Certain 2022 Lexus NX and Toyota Tundra vehicles' electronic parking brake systems may fail to engage because the Skid Control ECU falsely detects an overcurrent condition. This increases the risk of vehicle rollaway.
Yuboloo is recalling about 1,050 infant bath seats sold on Amazon.com from May to November 2021 because they fail to meet federal safety standards and can tip over in water, posing a drowning hazard to infants.
Kolan LLC is recalling about 100 Otter MOMO children's sandals sold on Amazon.com from March through April 2022 because the inner layer exceeds federal lead content limits. Lead can be toxic if ingested by young children.
The FDA is recalling INTERA 3000 implantable hepatic infusion pumps due to a malfunction causing higher-than-expected medication flow rates. Patients should contact their healthcare provider.
Tovala is recalling its Gochujang-Glazed Salmon Bowl meal (No. 18-A) because it contains an undeclared peanut allergen. The affected products were distributed nationwide to consumers.
Hamilton's HAMILTON-C6 intensive care ventilator status indicator board may become loose, allowing water or disinfectants to enter the device and cause technical faults that could force the ventilator into unsafe modes where patients breathe unassisted room air.
Getinge Servo ventilators may fail to deliver ventilation and stop functioning, potentially causing oxygen deprivation and serious harm to critical care patients.
Tovala is recalling approximately 3,340 Gochujang-Glazed Pork Chop Bowl meals distributed nationwide because they contain undeclared peanuts, which pose an allergy risk to consumers with peanut allergies.
Synapse Biomedical is recalling the NeuRx Diaphragm Pacing System External Pulse Generator due to a circuit board defect causing performance degradation, potentially leading to cardiac complications, breathing failure, or device shutdown.
Boston Scientific recalled 184 guide catheters manufactured with the wrong tip curve specification. Affected devices were distributed to Greece, France, Germany, Italy, Brazil, South Korea, and Russia, but not the U.S.
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier. The product was distributed nationwide and internationally.
Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.
AZO YEAST PLUS 20 CT has been recalled by Family Dollar Stores due to improper storage temperature conditions that violate CGMP requirements. The product was distributed nationwide from April through June 2022.
McKesson is recalling MedSource IV Start kits due to facility temperature excursions that may have compromised product effectiveness. Affected units were received between June and September 2021.
Enjoy Life Natural Brands is recalling Brownie Bites - Salted Caramel (4.76 oz) due to potential hard plastic pieces. Approximately 89,736 cases were distributed nationwide in the US and Canada.
81 kits of LeadCare II blood lead test devices were recalled because temperature exposure during storage may have impacted product effectiveness. The affected lots were received between June and September 2021.