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
George J Howe Company, Inc. is recalling 25-pound cases of sunflower seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple states.
George J Howe Company, Inc. is recalling 6/11oz Sunflower Seeds Salted due to the presence of undeclared cashew (a tree nut allergen).
CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.
BMW is recalling 428 vehicles from 2023-2025 due to a potential integrated brake system malfunction that may reduce braking power or disable stability controls.
Joy Gourmet Foods LLC. is recalling Joy Rose Lassi 16 oz. because the product was not adequately pasteurized, which may allow harmful pathogens to survive. The affected product was distributed in NY, NJ, and PA.
George J Howe Company is recalling 5# Sunflower Seeds C/NS due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across 24 states.
Honda is recalling 2026 Pilot and Passport vehicles because improperly tightened rear subframe bolts may lead to vehicle instability or detachment, increasing crash risk.
Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.
Joy Gourmet Foods LLC is recalling Joy Mango Lassi 16 oz. and 64 oz. beverages due to inadequate pasteurization, which may allow harmful bacteria to survive.
Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and in Barbados.
Joy Gourmet Foods LLC is recalling Joy Mango-Pina-Orange Lassi in 16 oz. and 64 oz. sizes because the product was not adequately pasteurized. The affected bottles have expiry dates between June 30 and July 30, 2026.
PReye LLC is recalling PReye Vitamin See Antioxidant Preservative Free Eye Drops distributed in Colorado due to lack of assurance of sterility. All unexpired lots are affected.
Intuitive Surgical recalls certain Da Vinci surgical system operative components due to a defective E-brake retainer pin that may fail to engage the E-brake, potentially causing uncontrolled motion and patient injury.
Joy Saffron Cardamom Lassi 16 oz. is being recalled because it was not adequately pasteurized. The product was distributed in New York, New Jersey, and Pennsylvania.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.
Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications.
Utz Quality Foods is recalling 1.5 oz and 2 oz bags of Dirty Brand Salt and Vinegar Potato Chips due to potential Salmonella contamination. The affected products were distributed across 32 states.
Spring & Mulberry Inc. is recalling Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects approximately 66,779 individual bars distributed nationwide.
Medline Industries is recalling Medline Convenience Kits (models DYNJ905503F and DYNJ905503G) that contain Arrow Kits with Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) topical applicators due to non-sterility caused by the presence of Aspergillus penicillioides fungal contamination.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and to Barbados.
Medline Industries recalls convenience kits containing 10mL polycarbonate colored syringes because design changes were made outside of FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes used in surgical procedures. The manufacturer identified unapproved design changes to the products that were not cleared by the FDA through the 510(k) process.