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
Cooper Tire is recalling specific Evolution Tour, Mastercraft, Hercules, Starfire, and Stratus tires due to an improper sidewall component that may cause tire deflation and tread separation.
Cain Food Industries is recalling 2,000 pounds of SLB-R Powder due to possible Salmonella contamination. The product was distributed in seven states.
Cain Food Industries is recalling 2,200 pounds of BETA P-130 due to possible Salmonella contamination. The product was distributed in seven states.
Anazao Health is recalling Fentanyl Citrate products because environmental sampling detected Talaromyces rotundus, a fungus, indicating a lack of processing controls.
Maintainer is recalling 2015-2019 Custom Body Heavy Rescue vehicles because unprotected air pressure control lines may cause unexpected brake application.
Oliver Travel Trailers is recalling 2017-2019 Elite II travel trailers because improperly tightened axle bolts may affect braking or cause wheel detachment.
Prevost is recalling 2020 X3-45 and H3-45 coach buses because driveshaft clamp bolts may not be properly tightened, which could cause loss of drive or a road hazard.
Foretravel is recalling 2020 Realm and iH45 vehicles because a brake relay valve defect may increase stopping distance, raising crash risk.
Mack Trucks is recalling 2020 Anthem, Granite, and Pinnacle vehicles because steering drag link connections may be improperly installed, risking loss of steering control.
Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because front shocks may separate, potentially causing a steering fluid leak and loss of power steering assist.
Forest River is recalling 2020 Georgetown and FR3 motorhomes because trailer hitch bolts may not be properly tightened, posing a crash risk while towing.
Chrysler is recalling 2005-2006 Dodge Viper vehicles because the Occupant Restraint Control module may inadvertently deploy air bags and seat belt pretensioners, increasing injury risk.
Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because a brake relay valve defect may cause extended stopping distances, increasing crash risk.
General Motors is recalling 2019-2020 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because excessive glue on the battery cable may cause electrical arcing, stalling, or fire.
Vinyard Fruit & Vegetable Co. is recalling 5LB bags of Red Dragon Blend mix due to potential Listeria monocytogenes contamination. The product was distributed in Oklahoma and Arkansas.
GE Healthcare is recalling Giraffe infant warmers because bedside panels and portholes may appear closed without being latched, posing a risk of patient falls.
Vinyard Fruit & Vegetable Co. is recalling 80003 Broccoli Cheddar Pasta Salad Kits due to potential Listeria monocytogenes contamination. The product was distributed in Oklahoma and Arkansas.
Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 150 mg because the FDA detected the NDMA impurity in the product.
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of glass particulate matter.
QuVa Pharma is recalling specific lots of fentanyl and bupivacaine infusions due to the potential presence of glass particulate matter.
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of particulate matter, including potential glass particles.
BMW is recalling 2019-2020 M5 and 2020 M8 vehicles because a damaged transmission wiring harness can cause an electrical short, leading to loss of propulsion and increased crash risk.
Ford is recalling 2017-2019 F-Super Duty trucks because seat belt pretensioner sparks could ignite B-pillar materials, potentially causing a vehicle fire.
Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 75 mg tablets nationwide because NDMA impurity was detected in the product.
Sanofi-Aventis U.S. LLC is recalling Maximum Strength Zantac 150 mg tablets nationwide because an NDMA impurity was detected in the product.