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 598 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 658 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Strides Pharma Inc. is recalling 49,488 bottles of Cinacalcet Tablets, 30 mg, because they failed dissolution specifications. The recall is classified as Class II.
Pritam International is voluntarily recalling 409,800 tubes of Brush Buddies Barbie toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
El Ruisenor De Mexico, Inc. is recalling almond flour packaged in 1lb, 5lb, and 50lb clear plastic units due to an undeclared almond ingredient.
Boston Scientific Cork, Ltd. is recalling 609 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 357 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Medline Industries is recalling C-section drapes with pouches because they are difficult to remove and leave adhesive residue on patient skin.
Boston Scientific is recalling 1,292 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 42 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 various peanut products due to an undeclared peanut allergen. The recall covers raw and roasted peanuts distributed primarily in California.
Viatris is recalling 21,620 bottles of Telmisartan and Amlodipine tablets because the Telmisartan content may exceed specifications.
Medtronic is recalling InterStim Percutaneous Extensions because selecting an incompatible lead or extension may prevent the system from working as intended, potentially delaying surgery or requiring replacement.
El Ruisenor De Mexico, Inc. is recalling 628 pounds of pecans in shell due to an undeclared allergen ingredient. The product was distributed primarily to California customers.
El Ruisenor De Mexico, Inc. is recalling Jovy Gummy Bears Regular because the product contains undeclared artificial food dyes.
Boston Scientific is recalling 7,945 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Sempio Food Services is recalling 150 cases of canned yellow peaches due to elevated lead levels. The product was distributed to Asian grocery stores in 11 states.
Axonics is recalling PNE Lead Implant Kits because included 10mL luer lock syringes may leak or break, posing a risk to users.
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 689 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Techno-Path is recalling Multichem AE quality control material because stability drift affects the Ammonia analyte, potentially delaying diagnostic results.
Medtronic is recalling NDI Passive Spheres because variation in reflective material may affect the navigation system's ability to detect and track the spheres.
El Ruisenor De Mexico, Inc. is recalling specific lots of whole wheat flour because the product contains an undeclared wheat allergen.
El Ruisenor De Mexico, Inc. is recalling 10X10 Wheat Snack because it contains wheat, an allergen not declared on the label.
El Ruisenor De Mexico, Inc. is recalling walnuts in shell because they contain an undeclared allergen. The product was distributed primarily in California and limited to other states.