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
G.O. Corporation is recalling Lettuce Salad Shred Mix due to potential contamination with deer feces. The affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.
Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer MIS Diamond-Touch Grasper surgical tool due to defects in the rotation knob adhesive that may cause cracking or breaking during use.
Carefusion is recalling specific lots of Snowden-Pencer MIS endoscopic surgical clamps due to potential cracking or breaking of the rotation knob caused by incorrect adhesive use during manufacturing.
Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.
Get Fresh Produce, Inc. is recalling Garden Cut Lettuce Greek Mix Salad (product number 10149) due to possible contamination with deer feces. Affected product was distributed in Illinois and Florida.
VEROCCA Locally Handmade Alfajor cookies are being recalled due to undeclared wheat, milk, and soybean oil allergens. Consumers with allergies to these ingredients should not consume the product.
G.O. Corporation is recalling Lettuce Salad Blend Monterey (Produce Code 404709) from Iowa, Minnesota, North Dakota, and Wisconsin due to potential contamination with deer feces. The recall affects 23,186 pounds across lot codes 130209 and 130212.
Trader Joe's Gluten Free Joe-Joe's Chocolate Vanilla Creme Sandwich Cookies are being recalled due to undeclared peanuts. The recalled product was distributed to stores in seven states.
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.
Specific lots of Snowden-Pencer surgical clamps may have rotation knobs that crack or break due to incorrect adhesive use in manufacturing. Eight units with lot numbers L22, B23, or C23 distributed in the US and Canada are affected.
Dilettante Chocolates recalled Dark Ginger Bulk Truffles from Washington retail stores because the display placard's allergen declaration fails to clearly identify milk. The product boxes have the correct label.
Dilettante Chocolates Inc is recalling caramels sold from display cases because the display placard's allergen statement is incomplete. The placard lists only 'Contains: Dairy' despite cream and butter being shown in the ingredients list.
Dilettante Chocolates is recalling Mocha Cafe Espresso Bulk Caramels sold at its Washington retail locations due to a display placard allergen declaration that states 'Contains: Dairy' instead of 'Contains: Milk,' though milk is listed in the ingredients.
Dilettante Chocolates recalls Mocha Cafe Dark Raspberry Bulk Truffles sold at retail stores in Washington due to incomplete allergen labeling on display placards. The product contains dairy but the allergen declaration is incomplete.
Blue Triton is recalling certain batches of Zephyrhills 100% Natural Spring Water 16.9 FL Oz bottles distributed domestically due to bromate levels exceeding EPA maximum contaminant limits. Consumers should discontinue use of affected batches.
Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.
Commercial Bakeries is recalling Trader Joe's Tiniest Chocolate Chip Cookies due to undeclared peanut. Consumers with peanut allergies should not consume this product.
Newly Weds Foods is recalling a pork roll cure product due to potential contamination with small metal pieces. Consumers who have this product should stop using it.
Newly Weds Foods is recalling Heller's Modern Cure in 50-lb quantities due to possible metal contamination. No illnesses have been reported.
Newly Weds Foods recalls a bacon cure product due to possible contamination with small metal pieces. Consumers who purchased this product should not use it.
Dilettante Chocolates is recalling Mocha Cafe brand Sriracha Bulk Caramels sold at Washington retail locations due to inconsistent dairy allergen labeling on display case placards versus case boxes.
Dilettante Chocolates recalls Mocha Cafe Espresso Bulk Truffles sold at Washington retail locations. The retail display placard's allergen statement declares 'Contains: Dairy' instead of the required 'Contains: Milk.'
Newly Weds Foods, Inc. is recalling its G25928 Curing Salt product because it may contain small pieces of metal. Affected consumers should not use this product.
Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.