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
The Kansas City Baking Company is recalling ready-to-eat meat products produced without federal inspection and containing undeclared allergens.
J Bar B Foods is recalling approximately 4,050 pounds of chicken sausage products because they contain milk, a known allergen, that is not declared on the label.
Medtronic is recalling 951 Compia MRI CRT-Ds because a defect may prevent the delivery of high and low voltage therapy.
Medtronic is recalling 951 Evera ICDs and CRT-Ds because a defect may prevent the devices from delivering high or low voltage therapy.
ABH Nature's Products is recalling Arthri-D 120ct bottles because they may be contaminated with Salmonella. The product was distributed directly to Massachusetts and Pennsylvania.
The Compounding Pharmacy of America is recalling 5 vials of HCG and Methylcobalamin injection due to non-sterility. The product was distributed in Tennessee and South Carolina.
Magno Humphries Laboratories is recalling Senna Laxative tablets that were mislabeled and contained Naproxen Sodium instead.
Productos Pacheco, Inc. is recalling Polvorones NET WT 4OZ due to undeclared soy and wheat allergens. The product was distributed to consignees in Puerto Rico.
Brenckle Farms is recalling fresh cilantro from Hartville, Ohio, after being notified that the product contains Listeria monocytogenes.
AuroMedics Pharma LLC is recalling 9,050 bags of Linezolid Injection 600 mg/300 mL because white particulate matter identified as mold was found in one bag.
Panera, LLC is recalling Plain Cream Cheese in 2 oz. and 8 oz. sizes due to potential Listeria monocytogenes contamination. The product was sold nationwide at Panera Cafes.
Panera is recalling Reduced-Fat Honey Walnut Cream Cheese due to potential Listeria monocytogenes contamination. The product was sold nationwide at Panera Cafes.
Panera, LLC is recalling Reduced-Fat Wild Blueberry Cream Cheese because it may be contaminated with Listeria monocytogenes. The product was sold nationwide at Panera Cafes.
Bulletproof 360 Inc is recalling Unflavored Collagen Protein because the product contains undeclared milk. The item is mislabeled as collagen protein but actually contains whey protein.
Aurobindo Pharma is recalling 53,040 vials of Ampicillin and Sulbactam for Injection due to a confirmed report of visible glass particulate matter.
AuroMedics Pharma LLC is recalling 66,100 vials of Pantoprazole Sodium for Injection because one vial contained a piece of glass.
Productos Pacheco, Inc. is recalling Vanilla Cake with Cheese due to undeclared allergens including wheat, soy, milk, and food dyes.
Panera, LLC is recalling Chive & Onion Reduced Fat Cream Cheese Spread due to potential Listeria monocytogenes contamination.
A&H Focal Inc. is recalling LANG YI HAO CHAONONGSUOPIAN tablets because they contain sildenafil without FDA approval. The products were sold in New York and New Jersey.
Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.
International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.
Premier Produce is recalling one lot of Jicama Julienne contaminated with Listeria monocytogenes. The product was distributed to U.S. consignees.
A&H Focal Inc. is recalling Zhonghua Niubian tablets found to contain sildenafil, an unapproved drug for erectile dysfunction.
Guymon Extracts Inc. is recalling approximately 4,202 pounds of fully cooked pork products due to a processing deviation that may have allowed pathogen growth.
BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.