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
Life Technologies is recalling 16 Ion Torrent Genexus Dx systems due to software vulnerabilities. The affected units are distributed in 11 US states.
Boston Scientific is recalling 1,135 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 8,542 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 1,212 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 797,868 tubes of Brush Buddies toothpaste nationwide due to CGMP deviations.
Boston Scientific is recalling 860 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Evexias Health Solutions is recalling Amino Ultra dietary supplements because the product is mislabeled and fails to declare fish oil.
Medline Industries is recalling 161 units of Drape C-SEC Fen Clear Screen Wire because the product is difficult to remove and leaves adhesive residue on patient skin.
Boston Scientific is recalling 926 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
El Ruisenor De Mexico, Inc. is recalling 21.20 pounds of apple rings due to undeclared sulfites. The product was distributed primarily in California and limited areas in six other states.
Pritam International is voluntarily recalling 320,232 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Boston Scientific is recalling 126 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling Brush Buddies My Little Pony toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
El Ruisenor De Mexico, Inc. is recalling 102 pounds of dried cod for containing an undeclared fish allergen. The product was distributed primarily to California customers.
El Ruisenor De Mexico, Inc. is recalling 411 pounds of sliced almonds due to an undeclared allergen ingredient. The product was distributed primarily to California customers.
Boston Scientific is recalling 112 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 86 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 389,880 tubes of evo Sensitive Anticavity Fluoride Toothpaste due to CGMP deviations.
Boston Scientific is recalling 39 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
El Ruisenor De Mexico, Inc. is recalling 192 pounds of dried whole shrimp because the product contains an undeclared allergen. The recall is classified as Class III.
Medline is recalling 222 C-Section Pack kits because they are difficult to remove and leave adhesive residue on patient skin.
El Ruisenor De Mexico, Inc. is recalling 26 pounds of Dried Diced Papaya because the product contains undeclared Yellow #6 and Sulfites.
Boston Scientific is recalling 486 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
El Ruisenor De Mexico, Inc. is recalling roasted whole almonds due to an undeclared almond allergen. The product was distributed primarily in California and limited areas in other states.
El Ruisenor De Mexico, Inc. is recalling Natural Sesame Seeds because the product contains undeclared sesame, a common allergen.