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
American Contract Systems is recalling Spine Pack convenience kits (Lot 980241) due to incomplete post-sterilization aeration. The affected kits were distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.
American Contract Systems Laparoscopy and Lap Chole surgical kits are being recalled because insufficient aeration time after sterilization may have compromised their sterility. The kits were distributed in seven U.S. states.
BD PYXIS MEDBANK automated medication dispensers may print incorrect medication bin labels due to a software defect, risking medication handling errors in healthcare settings.
Siemens recalled 24 units of the Luminos dRF Max X-ray display system because the support arm may unintentionally lower, potentially injuring personnel positioned beneath the equipment.
Panaderia Guatemex is recalling churros with undeclared soy allergen distributed in GA, KY, and TN. Consumers with soy allergies should not consume this product.
Philips IntelliVue patient monitors shipped or updated with software that removes monitoring capabilities, potentially delaying or resulting in incorrect treatment.
American Contract Systems is recalling 224 Biopsy Drape Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised the sterility of affected units. Lot 981241 distributed in CA, KS, ME, MN, MO, NE, and SD is affected.
Urban River Spirits is recalling Ruby-Red Grapefruit Mixer due to potential under-processing of the non-alcoholic beverage made in an unlicensed facility. No illnesses have been reported.
Urban River Spirits is recalling Lush Lavender & Wildberry Spritz non-alcoholic mixer due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.
Urban River Spirits Crisp Cucumber and Mint cocktail mixer recalled due to production in an unlicensed, uninspected facility. Potential under-processing poses a safety risk.
Urban River Spirits is recalling Watermelon Lemonade Splash non-alcoholic mixer due to potential under-processing. The product was manufactured in an unlicensed, uninspected facility, raising food safety concerns.
Urban River Spirits is recalling 3,876 bottles of Cinnamon Infused Simple Syrup due to manufacturing in an unlicensed, uninspected facility with potential under-processing concerns.
Olympus Corporation is recalling the Soltive Pro SuperPulsed Laser System due to difficulties pairing its wireless footswitch, which could delay surgical procedures. The recall affects 253 units worldwide.
Urban River Spirits is recalling Raspberry Lemon Mixer because the product was manufactured in an unlicensed and uninspected facility. The recall concerns potential under-processing issues.
Walgreen Co. is recalling Acetaminophen 500mg Rapid Release Gelcaps (Lot #31670346AA, expires 12/31/2026) due to incorrect carton labeling. The 21,192 affected bottles were distributed to retailers in Illinois.
Urban River Spirits' Spicy Orange and Mango Fusion non-alcoholic cocktail mixer is recalled due to production in an unlicensed, uninspected facility with potential under-processing. Approximately 3,876 bottles were distributed across 11 states.
Urban River Spirits is recalling Brown Sugar Simple Syrup due to manufacture in an unlicensed, uninspected facility with potential under-processing concerns.
Urban River Spirits is recalling 3876 bottles of Blackberry and Lime Mixer manufactured in an unlicensed, uninspected facility with potential under-processing. Consumers across 11 states should not consume the product.
Urban River Spirits recalled Keep It Spicy Pear & Jalapeno Mixer because it was produced in an unlicensed, uninspected facility with potential under-processing. The product was distributed across 11 states.
Urban River Spirits Vanilla Infused Simple Syrup is being recalled. The product was made in an unlicensed and uninspected facility with potential under-processing, raising food safety concerns.
Cafe Caramel Delight, a non-alcoholic cocktail mixer, is being recalled because it was produced in an unlicensed, uninspected facility with potential under-processing concerns.
Urban River Spirits is recalling 3,876 bottles of Spicy Cool-aid: Watermelon & Jalapeno due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.
Urban River Spirits is recalling Peppered Peach Bliss, a non-alcoholic cocktail mixer, due to potential under-processing risks. The product was manufactured in an unlicensed and uninspected facility.
Frozen Food Processors recalls frozen cornbread muffins manufactured without state license and in unsanitary conditions. The recall affects approximately 1,862 cases distributed in MS, TN, LA, AR, and AL.
Urban River Spirits is recalling its Lemon Drop Mixer due to being manufactured in an unlicensed, uninspected facility with potential under-processing concerns affecting product safety. The product was distributed across multiple states.