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
PD-Rx Pharmaceuticals is recalling 1,683 bottles of Metformin Hydrochloride Extended Release 500 mg because of NDMA impurity levels above acceptable limits.
Zimmer Biomet is recalling 412 acetabular hip cup components because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Time-Cap Labs, Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 500 mg because the FDA detected the impurity N-Nitrosodimethylamine (NDMA) above acceptable intake levels.
Marksans Pharma Limited is recalling Metformin Hydrochloride Extended Release tablets due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.
Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because the drive shaft may fracture, potentially causing a loss of drive, vehicle rollaway, or fire.
Jaguar Land Rover is recalling 2019-2020 Discovery vehicles because a loose battery ground stud may cause electrical power loss or vehicle shutdown while driving.
Ford is recalling 2014-2016 Explorer, 2014-2015 Taurus, and 2014 Edge vehicles because a front drive axle bracket may fail, risking loss of park function or motive power.
Sunjoy is recalling Oakmont LP fire pit tables sold at Big Lots because an incorrectly installed hose can melt and ignite, posing a fire hazard.
Kohl's is recalling approximately 512,000 SONOMA Goods For Life three-wick candles because high flames can ignite wax or break glass, posing fire and burn risks.
Winnebago is recalling certain 2021 Micro Minnie trailers equipped with undersized axles that may break under the vehicle's weight, potentially causing serious injury or death.
Ring is recalling approximately 350,000 2nd Generation Video Doorbells because incorrect installation screws can cause the battery to overheat, posing fire and burn risks.
Autocar is recalling 2020-2021 Xpeditor and Legend vehicles because transverse torque rod mounting bolts may not be properly tightened. If bolts fail and disconnect, vehicles could lose suspension control, increasing crash risk.
Forest River is recalling 2019-2020 Rockport work trucks because the battery box may be inadequately welded and detach, increasing crash risk.
Daimler Trucks North America is recalling 2019-2021 Freightliner Econic SD vehicles because damaged electrical cables may cause a fire or engine stall.
Jaguar Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque MHEV vehicles because an electrical short-circuit could cause a fire.
Wawona Packing Co LLC is recalling field run peaches because FDA sampling found Salmonella in the fruit and leaves.
Certain 2020-2021 BMW X5, X6, X7, and related models have a front axle support weld that may separate, potentially affecting vehicle handling and control and increasing crash risk.
Bausch Health is recalling 35,424 tubes of Hydrocortisone butyrate Cream, 0.1%, because the product was found to be subpotent.
RemedyRepack Inc. is recalling Metformin Hydrochloride Extended Release 750 mg tablets because of detected NDMA impurity levels above acceptable intake limits.
W L Gore is recalling GORE TAG CONFORMABLE Thoracic Stent Grafts because a secondary deployment fiber attachment prevented completion of deployment via the access hatch.