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
Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.
Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.
Caire, Inc. is recalling 10 CAIRE Liberator 45 liquid oxygen system units due to inconsistencies in weld penetration on the inner bottle discovered during an FDA audit.
GREEN DAY PRODUCE is recalling enoki mushrooms (UPC 16430-69080) due to Listeria monocytogenes contamination. Affected products were distributed to retailers and distributors in 12 states.
Remel's Sensititre STP6F diagnostic plates may produce false susceptible results for Gram-negative bacteria when tested with certain antibiotics, potentially leading to inappropriate treatment decisions.
Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.
Remel Inc. recalled 8,073 units of Sensititre GN7F antibiotic susceptibility test plates after discovering they may report false results for certain bacteria, potentially leading to incorrect antibiotic treatment decisions.
Boston Baking Mini Crumb Cake (3 oz, individually wrapped) is recalled for undeclared pecans. The product was distributed in six northeastern states and may pose a serious risk to consumers with tree nut allergies.
Dewei DNA/RNA Preservation Kits (catalog DW-80005-1B) were distributed in the U.S. without FDA authorization or clearance. Approximately 1,348,000 units were distributed to California, Florida, Kentucky, and Michigan.
A retaining ring on the 2021 Porsche Taycan's suspension strut may come loose, causing loss of vehicle control and increasing crash risk. Repairs will be provided free by Porsche dealers.
McLaren is recalling 164 2023 Artura vehicles because high-pressure fuel pipe nuts may loosen, causing fuel leaks that could lead to fires. Dealers will replace the fuel pipes at no cost.
Kia is recalling certain 2023 Forte vehicles due to a manufacturing error that may cause the front left steering knuckle to crack, resulting in loss of steering control and increased crash risk.
3M is recalling approximately 516,500 Scotch TL1302 Thermal Laminators because a safety feature can malfunction when the device overheats, posing a fire hazard. The company has received nine reports of the laminators catching fire, with three reports of minor property damage but no injuries.
Ortal USA is recalling about 400 Traditional 90 and Traditional 110 gas fireplaces due to improper installation that can cause fire hazards. The firm has received four reports of installation errors resulting in fires with property damage.
Choi Heong Yuen Bakery Almond Cakes may contain undeclared milk. Consumers with milk allergies who purchased this product should stop consuming it and contact the manufacturer.
eWheels LLC is recalling about 500 Gotway and Begode electric unicycles because their lithium-ion batteries can ignite, creating a fire hazard. Fourteen fire incidents have been reported, including property damage and one injury.
DAISO CALIFORNIA WAREHOUSE is recalling Tiramisu Twist Cookie 3.4 oz. packages due to undeclared tree nuts. Consumers with tree nut allergies face allergic reaction risk if they consume this product unknowingly.
Umami Everyday Sauce is being recalled due to undeclared soy allergen. This poses a risk to consumers with soy allergies and sensitivities.
Seed Ranch Flavor Co. is recalling Everything But The Sushi & Dumplings sauce due to undeclared soy allergen. Approximately 11,449 bottles were distributed nationwide and internationally.
3M is recalling Steri-Drape surgical drapes due to a defective adhesive liner that is difficult to remove and may render the drape unusable. Reported adhesive-related skin injuries have been linked to the affected lots.
3M is recalling approximately 14,360 units of Steri-Drape surgical drapes due to adhesive-related skin injuries. The product's adhesive liner is difficult to remove and may render the drape unusable.
Whele LLC is recalling the Mighty Bliss Electric Heating Pad (model MB-001) due to burn and electrical shock hazards. The firm has received complaints of burns, shocks, and skin rashes from users.
3M is recalling 103,000 units of Steri-Drape surgical drapes worldwide due to difficulties removing the adhesive liner and an increase in reported skin injuries from the adhesive.
Whele LLC is recalling approximately 4,034 Mighty Bliss Electric Heating Pads due to burn and shock hazards. The firm received complaints of burns, mild electrical shocks, and skin irritation.
Nourish Inc. Fruit Snack Pack SNACK ATTACK recalled for undeclared peanut allergen. 188 units distributed to 4 customers in California.