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
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming salmonella contamination.
Gaia Ethnobotanical LLC is recalling Red Dragon Kratom powder due to Salmonella contamination found by FDA analysis.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA analysis confirming Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Green Dragon Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.
Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling various Gaia Kratom powder products nationwide due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
AuroMedics Pharma LLC is recalling 73,620 vials of Piperacillin and Tazobactam for Injection due to the presence of glass and silicone particulate matter.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling White Borneo Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.
Gaia Ethnobotanical LLC is recalling White Thai Kratom powder due to FDA-confirmed Salmonella contamination.
Akorn, Inc. is recalling 89,507 vials of Acetylcysteine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is classified as FDA Class II.