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
Badger Botanicals LLC is recalling specific Kratom products due to potential Salmonella contamination.
Triangle Pharmanaturals LLC is recalling Molecule Kratom Gold Bali products because they may be contaminated with Salmonella.
Triangle Pharmanaturals LLC is recalling Naturally Kratom Green Malay capsules due to potential Salmonella contamination. The product was distributed in 24 states.
Triangle Pharmanaturals LLC is recalling Lifted Kratom Green Maeng Da products due to potential Salmonella contamination.
Triangle Pharmanaturals LLC is recalling Lifted Kratom White Maeng Da products due to potential Salmonella contamination. The recall covers powder and capsule bottles distributed in 24 states.
Triangle Pharmanaturals LLC is recalling Chameleon Kratom Formula 27 capsules due to potential Salmonella contamination. The product was distributed in 24 states.
Triangle Pharmanaturals LLC is recalling Molecule Kratom White Borneo products in various formats due to potential Salmonella contamination.
Maya Distribution, LLC is recalling Dragon Malaysian Kratom products because samples tested positive for Salmonella. The products were distributed to retail stores in eight states.
Triangle Pharmanaturals LLC is recalling all Kratom products due to potential Salmonella contamination. The recall covers Raw Form Organics Maeng Da Kratom Ruby Red capsules.
Triangle Pharmanaturals LLC is recalling Third Eye Kratom Bali capsules because all Kratom products from the firm may be contaminated with Salmonella.
Triangle Pharmanaturals LLC is recalling Live Well Kratom Green Maeng Da capsules in 150 and 300-count bottles due to potential Salmonella contamination.
Maya Distribution, LLC is recalling Dragon Ultra Enhanced Indo Extract capsules because samples tested positive for Salmonella.
Greenbelt Greenhouse Ltd is recalling Spicy Microgreen Mix due to potential Listeria monocytogenes contamination. The product was distributed in Oregon and Washington.
Triangle Pharmanaturals LLC is recalling Molecule Kratom Super Green Malay products because they may be contaminated with Salmonella.
McNeilus is recalling 2008-2018 Bridgemaster V concrete mixers because a hydraulic tank may overpressurize and rupture, posing risks of injury and road hazards.
Vyaire Medical is recalling 20 AirLife Resuscitation Broselow Hinkle Kits because the mask component may stick, making it difficult to disconnect from the device.
Vyaire Medical is recalling 198 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Vyaire Medical is recalling 24 AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Vyaire Medical is recalling 18 AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Vyaire Medical is recalling 6 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Vyaire Medical is recalling 180 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Datascope Corporation is recalling three units of the Adult ECC Pack BEQ-TOP 22300 because seal separation may allow air into the housing, potentially collapsing the balloon and reducing blood flow.
Vyaire Medical is recalling 8,058 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Kroger Specialty Pharmacy is recalling Glatiramer Acetate 40 mg/mL due to a lack of processing controls. The affected product was dispensed in five states.
Kroger Specialty Pharmacy is recalling Xtandi 40 mg capsules due to a lack of processing controls. The affected products were dispensed in five states.