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
Paradise Flavors LLC is recalling Blackberry Cheesecake ice cream (4 oz) due to undeclared milk, soy, and wheat allergens. The product was distributed in Florida.
Paradise Flavors recalls Sweet Corn ice cream mix distributed in Florida for undeclared milk allergen and color additives. Consumers with milk allergies risk allergic reaction from this product.
YOGOBERRY frozen yogurt (4 oz pouches) is recalled due to undeclared allergens: milk, tree nuts, peanuts, soy, and wheat. The product was distributed in Florida.
Paradise Flavors LLC has recalled its 4 oz Pine Nut Ice Cream Bar due to undeclared allergens: milk, tree nuts, soy, and wheat. The product was distributed in Florida and poses a risk to consumers with these allergies.
Paradise Flavors LLC is recalling Cotton Candy with M&Ms due to undeclared milk, peanuts, and soy allergens, plus undeclared color additives. The product was distributed in Florida.
Paradise Flavors LLC is recalling frozen chocolate ice cream (4 OZ/120 ML packages) distributed in Florida due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Paradise Flavors is recalling its 4 oz Guavanana (soursop) ice-cream base because it contains undeclared milk, a major allergen that poses health risks to consumers with milk allergies.
Paradise Flavors is recalling pistachio ice cream base (4 oz pouches) distributed in Florida due to undeclared milk and tree nuts. The product also contains undeclared color additives FD&C yellow #5 and blue #1.
Paradise Flavors is recalling 86 units of frozen guava jelly ice-cream product due to undeclared milk allergen and color additives (FD&C yellow #5, yellow #8, red #40). The product was distributed only in Florida.
Paradise Flavors LLC is recalling Trail Mix/Frutas Secas ice cream base because it contains undeclared allergens: milk, tree nuts, peanuts, and soy. Consumers with allergies to these ingredients should not consume the product.
Paradise Flavors Arroz con Leche rice pudding ice cream mix is recalled due to undeclared milk allergen. Consumers with milk allergies should not consume this product.
Paradise Flavors LLC recalls its frozen avocado ice-cream base for undeclared milk allergen and FD&C color additives. The product was distributed in Florida and may pose a risk to milk-allergic consumers.
Paradise Flavors is recalling 120 units of Pina Colada ice-cream base in 4 oz packages due to undeclared milk and tree nuts allergens, and undeclared color additives. Consumers with allergies should not consume this product.
Medline is recalling 1,770 Peripheral Blood Culture Draw kits because components within the kits have expired before the kit's stated expiration date.
A software defect in Philips Big Bore RT CT scanners may cause incorrect coordinates in radiation therapy planning systems, affecting 56 units distributed nationwide and internationally.
Physio-Control LIFEPAK 15 defibrillators (serial numbers 48433670 and 48744028) may experience battery pin loosening, potentially causing power issues. Two units were distributed in AZ, CA, NC, NJ, and NY.
Medline Industries is recalling 1,600 Central Line Blood Culture kits due to component expiration prior to the listed kit expiration date. Expired materials could compromise blood culture test accuracy.
Tay's Sales and Distribution is recalling Full Spectrum Cold Pressed Hemp Oil Gummies because sunflower butter sub-ingredients were not declared on the label. Consumers with sunflower allergies may experience allergic reactions.
Amazon Fresh Frosted Mini Brownies (Item 19858) may contain plastic pieces. The 12-count packs distributed nationwide are subject to recall.
Family Medical Supply Inc is recalling 26,657 cylinders of compressed oxygen distributed nationwide due to manufacturing practice deviations. Cylinders were manufactured between May 10 and October 31, 2023.
Atrium Medical Corporation is recalling 141 units of the Advanta V12 Covered Stent System due to a balloon-to-catheter weld failure that may cause loss of balloon pressure during stent deployment. Affected units were distributed to eleven countries.
Philips Brilliance CT Big Bore units with software V4.8.0.10421 may produce inaccurate image position data when offset reconstruction is used. This could lead to incorrect radiation therapy planning or diagnosis.
Philips is recalling the Spectral CT on Rails (Model 728334, Software Version 5.1.0) due to a software crash that occurs when CCT Fluoroscopy mode and foot pedal are activated simultaneously. The crash requires system restart.
Medline is recalling 4,850 adult blood culture collection kits (lot numbers 23EMI373, 23EMF712, 23DMF155, 23CMH026) because components inside expired before the kit's labeled expiration date.
Microbiologics Inc recalls KWIKSTIK microbiological reagent kits due to Aspergillus flavus contamination in bulk pellets. Affected products were distributed worldwide, including the US, Italy, France, Turkey, Peru, and Mexico.