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
Forest River is recalling 2018-2019 Glaval Bus models because the roof hatch handle may break, preventing emergency exit.
Piaggio is recalling 2019-2020 Vespa scooters because improperly galvanized brake lines may release hydrogen, reducing braking ability and increasing crash risk.
Chrysler is recalling 2015-2018 Ram ProMaster vans because a seizing engine cooling fan can overheat and cause a fire. Owners should contact dealers for a free replacement.
Chrysler is recalling 2012-2013 Fiat 500 vehicles with 6-speed automatic transmissions because a shifter cable bushing may fail, allowing the cable to detach.
Mercedes-Benz is recalling 2018-2019 S560 vehicles because an improperly tightened engine part may detach, causing a stall and increasing crash risk.
General Motors is recalling specific 2019-2020 Chevrolet Silverado and GMC Sierra trucks because hot gas from seat belt pretensioners could ignite the carpet, causing a vehicle fire.
Chrysler is recalling Mopar steering assemblies for Ram 1500 trucks because a contaminated circuit card may short circuit, causing intermittent loss of power steering assist.
Ioxus Corporation is recalling 12V uSTART MD battery support modules because internal short circuits can cause vehicle fires.
Chrysler is recalling 2011-2013 Jeep Grand Cherokee and Dodge Durango vehicles because a fuel pump relay may fail, causing the vehicle to stall without warning and increasing crash risk.
Chrysler is recalling 2019 Ram 1500 trucks because a contaminated electric power steering gear may short circuit, causing intermittent loss of steering assist.
Green Lumber Holdings is recalling Natural Fuel For Men capsules because FDA analysis found undeclared Tadalafil, an approved drug for erectile dysfunction.
Wawona Frozen Foods is recalling specific frozen berry products after FDA sampling detected Hepatitis A. Consumers should check their freezers for the listed items and dates.
Jumbo Foods is recalling Tuscan Sun brand Wedge Chicken Salad sandwiches due to potential Listeria monocytogenes contamination. The product was distributed to stores in eight states.
Jumbo Foods is recalling Tuscan Sun Cranberry Chicken Salad sandwiches due to potential Listeria monocytogenes contamination. Affected products were distributed in eight states.
Azuma Foods International is recalling Teriyaki Grilled Calamari due to presumptive positive test results for Listeria monocytogenes.
Wawona Frozen Foods is recalling frozen raspberries sold at Aldi and Raley's because FDA sampling found Hepatitis A. Consumers should check their bags for specific dates and codes.
Baxter is recalling Prismaflex Control Units with software below version 7.21 due to communication errors that may interrupt therapy or cause blood loss.
Dr. Reddy's Laboratories is recalling Ranitidine Tablets 75 mg because of the presence of the NDMA impurity.
Baxter is recalling Prismaflex Control Units with software below version 7.21 due to communication errors that may interrupt therapy or cause blood loss.
Philips Medical Systems is recalling 1,167 Forte Gamma Camera Systems because a detector may fall vertically to the end stops of its travel limit.
Red Mountain Compounding Pharmacy is recalling S-TEST CYP 125mg/ml vials due to a lack of assurance of sterility.
Dr. Reddy's Laboratories is recalling Ranitidine Tablets 75 mg because of the presence of the NDMA impurity.
Medtech SAS is recalling 93 Rosa Brain 3.0 neurosurgical devices because the instrument holder may send tools on incorrect trajectories, potentially leading to improper device placement.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Lidocaine HCL 2% Injection because the product lacks assurance of sterility.
Baxter Healthcare is recalling Prismaflex Control Units with software versions below 7.21 because communication error alarms may interrupt therapy or cause blood loss.