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
Boston Scientific is recalling 382 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 237 pounds of whole wheat flour due to an undeclared wheat allergen. The product was distributed primarily in California and limited areas in six other states.
El Ruisenor De Mexico, Inc. is recalling Jovy Watermelon Gummy Rings because they contain the undeclared allergen Red #40.
Medline is recalling 108 C-Section Tray kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Medtronic is recalling InterStim SureScan MRI Leads because selecting an incompatible lead or extension prevents the system from working as intended.
Medline Industries is recalling 10 FETOSCOPY CDS-LF medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Pritam International is voluntarily recalling Brush Buddies toothpaste nationwide due to CGMP deviations. No illnesses or injuries are reported.
Gearharts Fine Chocolates is recalling 4,703 pieces of chocolate because broken glass was found in finished product. The recall covers 4oz and 8oz packages shipped to 17 states.
El Ruisenor De Mexico, Inc. is recalling ground shrimp because it contains an undeclared allergen. The product was distributed primarily in California and limited areas in other states.
Pritam International is voluntarily recalling 15,264 tubes of ARU Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations. The product was distributed nationwide in the US.
El Ruisenor De Mexico, Inc. is recalling 2,231 pounds of Whole Wheat packaged in 1lb, 5lb, and 50lb clear plastic units due to an undeclared wheat allergen.
Ascend Laboratories is recalling 11,424 bottles of Amlodipine and Olmesartan Medoxomil tablets because they failed to meet dissolution specifications.
Boston Scientific is recalling 2,547 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Solstice Corporation is recalling 736 Xact mole markers for mammography because the radiopaque material may detach, causing imaging artifacts.
El Ruisenor De Mexico, Inc. is recalling hazelnuts in shell because the product contains an undeclared allergen. The recall covers 1lb, 5lb, and 50lb bags distributed primarily in California.
Boston Scientific Cork, Ltd. is recalling 228 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pacific Coast Producers is recalling Great Value Fruit Cocktail due to potential contamination with elevated levels of lead.
Boston Scientific is recalling 384 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 112,092 tubes of Brush Buddies toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Boston Scientific is recalling 3,145 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Abbott is recalling Amplatzer Amulet Left Atrial Appendage Occluder devices to update instructions for use regarding the risk of pulmonary artery injury.
restor3d Inc. is recalling 16 restor3d MTP Implants because field findings showed orange sterilization indicators, meaning the devices were not exposed to sterilization.
Boston Scientific is recalling 156 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 620 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Medline Industries is recalling 26,965 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.