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
Keystone Industries recalls Ipana 20% Benzocaine Topical Gel due to a manufacturing quality issue. The bulk product was released from a mixing vessel with scratches despite Quality Unit rejection.
Gelato Benzocaine 20% topical anesthetic (Lot BNZ-001646) is recalled due to scratches found in the mixing vessel during manufacturing. The defective product was inadvertently released despite quality control rejection, though no illnesses have been reported.
Keystone Industries recalls Burkhart Topical Anesthetic Gel due to CGMP deviations discovered during quality inspection. The product was inadvertently released despite being flagged for rejection.
Augustine Temperature Management is updating instructions for HOT DOG Patient Warming Controllers (Models WC71, WC71R) regarding a power-on self-test error code. The update affects 135 units distributed in the US and Canada.
Keystone Industries is recalling one lot of Patterson Dental Topical Anesthetic due to manufacturing quality deviations. The product was shipped despite being marked for rejection due to scratches in the mixing vessel.
Augustine Temperature Management is issuing an instructions for use update for its HOT DOG warming controllers (Models WC77, WC77D, WC77R) regarding a power-on self-test error code.
Charmast W1056 power banks sold on Amazon.com from December 2018-September 2024 are recalled for lithium-ion battery fire and burn hazards. The company received 44 reports of overheating, ignition, or burns.
SKIL 40V batteries sold from 2019–2024 can overheat, causing fires and burns. Chervon reports 100 thermal incidents, including 8 burn/smoke cases and 49 property damage claims.
Elongdi magnetic building stick sets sold on Amazon are recalled due to violation of federal toy magnet regulations. When swallowed, the high-powered magnets can attract each other and lodge in the digestive system, potentially causing serious internal injuries.
Melii Baby silicone spoons for babies can break apart during use, creating a choking hazard. About 85,100 units sold through multiple retailers from April to August 2024 are affected; consumers should stop using them immediately.
4Earth Farms is recalling 6,036 cases of broccoli medley due to potential contamination with E. coli O121:H19. The product was distributed to retailers and distribution centers across multiple states.
Con Yeager Spice Company is recalling Trail Bologna Meat Processing Kits because they contain undeclared wheat and soy allergens. Affected consumers with allergies should not consume the product.
4Earth Farms is recalling Organic Broccoli Medley packages due to potential E. coli O121:H19 contamination. The product was distributed across multiple states to retail and distribution centers.
4 Earth Farms Stir Fry Medley vegetables are being recalled due to potential E. coli O121:H19 contamination. The affected product was distributed to retailers across multiple states; consumers should not eat the product and should discard it.
4Earth Farms is recalling Organic Broccoli Slaw for potential E. coli O121:H19 contamination. Products were distributed to retail and distribution centers across multiple states.
Walmart is recalling Marketside Fresh Cut Cucumber Slices sold in Texas due to potential Salmonella contamination. Consumers should not eat this product and should return or dispose of it.
Sysco Corporation is recalling whole and cut cucumbers distributed in the Midwest and Canada due to potential Salmonella contamination.
4 Earth Farms is recalling Vegetable Medley due to potential contamination with E. coli O121:H19. Approximately 6,036 cases were distributed across multiple states.
4 Earth Farms is recalling Organic Vegetable Medley packages due to potential contamination with E. coli O121:H19. The affected products were distributed across multiple states to distribution centers and retailers.
4 Earth Farms is recalling Organic Vegetable Medley (Broccoli, Carrots & Cauliflower) sold at Walmart due to potential contamination with E. coli O121:H19. The recall affects 6,036 cases distributed across multiple states.
4 Earth Farms is recalling its 32-oz Vegetable Medley product distributed by Walmart due to potential contamination with E. coli O121:H19. The product was distributed to retail locations across multiple states.
F&S Produce West LLC is recalling Mediterranean Party Trays (sell-by dates 11/27/2024–12/11/2024) due to potential Salmonella contamination in the tzatziki sauce. The product was distributed to 187 retail locations in seven western states.
4Earth Farms is recalling 6,036 cases of organic carrots distributed across multiple states due to potential E. coli O121:H19 contamination.
Mylan Institutional is recalling 2,835 cartons of Levothyroxine Sodium 100 mcg tablets nationwide due to potency deviations—some tablets may be underdosed while others may be overdosed.
Micro-X Ltd. is recalling five MICRO-X Rover Mobile X-ray Systems due to a timing defect that prevents adequate X-ray exposures. The 4 millisecond exposure time does not allow sufficient tolerance for diagnostic-quality imaging.