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
Lamborghini is recalling 2015-2020 Huracan vehicles because missing caps on headlight adjustment screws can lead to improper alignment, reducing visibility and increasing crash risk.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because incorrect software may cause the airbag warning light to malfunction, potentially masking actual system failures.
Intermotive is recalling 514 Programmable Relay Power Center modules because exposed copper may cause short-circuits, increasing the risk of a fire.
Weldon is recalling specific rear combination lamps because the LED backup lights are the wrong color, failing federal safety standards and potentially affecting vehicle visibility.
Chrysler is recalling 2017-2018 Pacifica Plug-In Hybrid vehicles because a fire can occur while parked. Owners should park outside and avoid recharging until repairs are completed.
Mercedes-Benz is recalling 2021 GLB 250 vehicles because an incorrect front driver's air bag module may not restrain occupants or could detach during a crash.
Autocar is recalling 2020-2022 Legend vehicles because the grille bezel may detach, creating a road hazard and increasing crash risk.
Great American Cobbler LLC is recalling Creole Style Chicken Pot Pie products because they contain soy, a known allergen, that is not declared on the label.
BRP U.S. Inc. is recalling about 1,300 2022 Can-Am Outlander ATVs because the speedometer can display half the vehicle's true speed, creating a crash hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.
Serta is recalling about 800 Perfect Sleeper mattresses because they fail to meet federal flammability standards, creating a fire hazard. No injuries have been reported.
Thor Motor Coach is recalling 2022 ACE, Freedom Traveler, Hurricane, and Windsport motorhomes. The rear ladder may have been installed on the wrong side, which could break while in use and cause injury.
Positec USA is recalling about 17,630 WORX Brand 13 Amp 1900 PSI Electric Pressure Washers because the sprayer hose can separate from the spray wand during use, posing an impact injury hazard. Four minor injuries including cuts and bruises have been reported.
Ideal Specialty Apothecary is recalling Medroxyprogesterone Acetate Injection due to lack of assurance of sterility. The recall affects approximately 57,994 vials distributed nationwide.
Baxter is recalling 146,502 SIGMA Spectrum infusion pumps due to potential medication delivery failures that may occur without alerting clinicians. The issue is linked to administration set setup and occlusion alarm resolution.
Baxter Healthcare is recalling 241,304 Spectrum IQ infusion pumps due to potential medication delivery failure without user alert. The issue may occur during administration set setup or when occlusion alarms are not fully resolved.
CovClear COVID-19 Rapid Antigen Test kits (284,575 units) were distributed nationwide without FDA marketing approval, clearance, or authorization. All lots are recalled.
Empowered Diagnostics LLC recalled COVID-19 test kits (ImmunoPass, NAB 900-60) sold nationwide without FDA approval. Approximately 2,100 units were distributed without required marketing clearance or authorization.
OXY-1 System consoles used during cardiac support procedures may experience power interruptions that disrupt patient therapy, potentially causing prolonged oxygen deprivation.
Altec is recalling 2018-2021 Aerial Devices and Digger Derricks because cracks in the subbase bulkhead plate can cause shear plate failure, increasing the risk of injury.
Medline Industries is recalling 34 units of the Premier Rotaclone (Lot 696004N116) due to improper storage in temperature-controlled settings instead of required refrigeration. This may affect device performance or safety.
Delizza Belgian Mini Chocolate Cream Puffs are recalled due to small metal pieces found in the bakery's palm oil silo that could not be reliably detected by the manufacturer's metal detector system.
Home Easy is recalling about 3,000 Geek Heat DH-QN06 personal heaters because the toggle power switch can spark and cause a fire. The company has received three reports of fires caused by the switch, though no injuries or property damage have been reported.
DIXI Medical Microdeep Depth Electrodes are recalled due to potential deformation of the blister pack packaging that could compromise the sterile barrier. 345 units nationwide are affected.
DIXI Medical is recalling 484 Microdeep Depth Electrodes nationwide due to potential deformation of internal packaging that could compromise the sterile barrier of these brain recording devices.
Immuno-Mycologics recalls 411 Cryptococcal Antigen test kits (lots F1021035, F1021036) for reduced specificity (90% vs. 99%), which may cause false-positive results leading to unnecessary anti-fungal therapy.