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
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because non-flexible wiring in the bedroom slide-out may damage and cause a fire.
E-One is recalling 2016-2017 Cyclone II emergency vehicles because stress fractures in the aerial ladder tubing could cause failure and injure the bucket occupant.
Triple E RV is recalling 2017-2018 Wonder recreational vehicles because water can corrode wiring in the trailer tow module, potentially causing electrical shorts, fire, or crash risks.
Texas Natural Meats is recalling approximately 489 pounds of frozen raw ground beef products that may be contaminated with Shiga toxin-producing E. coli (STEC) O103.
Pious Lion is recalling Pink Bali products in North Carolina and Tennessee after the North Carolina Dept. of Agriculture notified the firm that the product contains Salmonella.
Sun Med, LLC is recalling 361 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach and impacting air delivery.
Inopak Ltd is recalling Option Systems Antibacterial Foaming Hand Wash because FDA analysis found out-of-specification microbial counts.
Angiodynamics Inc. is recalling 13 boxes of RS Tandem 5F DL Xcela PICC catheters because a component may contain unsafe levels of bacterial endotoxins.
TRW is recalling air bag control units in certain Hyundai and Kia vehicles because electrical overstress may prevent air bags and seat belt pretensioners from deploying in a crash.
Angiodynamics Inc. is recalling 2 boxes of CAN 5F DL BIOFLO PASV PICC Nursing Trays because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 5F DL BIOFLO PICC kits because a component may contain unsafe levels of bacterial endotoxins.
Philips is recalling two Brilliance 16 CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.
Pious Lion is recalling 4 oz bags of White Maeng DA Kratom because the North Carolina Department of Agriculture found the product contains Salmonella.
Angiodynamics Inc. is recalling 17 boxes of CAN 5F SINGLE XCELA PICC kits because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 3 boxes of RS - TANDEM 5F DL BIOFLO MIDLINE catheters because a component may contain unsafe levels of bacterial endotoxins.
Angiodynamics Inc. is recalling 298 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.
Philips is recalling 20 Brilliance 16 P CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.
Shadow Holdings DBA Bocchi Labs is recalling the Acne Shave 3 Step Shaving System due to CGMP deviations that may result in bacterial contamination.
Medline Industries is recalling specific lots of READYFLUSH PROTECT flushable personal cleaning cloths because of microbial contamination in a non-sterile product.
Sun Med, LLC is recalling 113 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach during use.
Allergan is recalling Taytulla softgel capsules because the tablets are out of sequence. This affects 168,768 blister cards distributed nationwide.
Angiodynamics Inc. is recalling 17 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.
The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle could fail, posing a risk of serious injury or death.
Angiodynamics Inc. is recalling BioFlo PICC nursing kits because a component may contain unsafe levels of bacterial endotoxins.