Hazard
395 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 395 mislabeling recalls we have scored against our rubric, 20 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 45 (11%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mislabeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Chicago Sweet Connections Paczkis (Raspberry Flavor) are recalled because they contain undeclared egg, milk, and wheat allergens. Consumers with allergies to these ingredients should not consume the product.
Chicago Sweet Connections: Paczkis - Cherry Flavor 4-packs contain undeclared egg, milk, and wheat allergens. Consumers with allergies should not consume this product.
BioPro Titanium MPJ toe implants are being recalled due to incorrect statements in device labeling claiming MR Conditional status when MR testing was not performed on the titanium version.
ROi CPS LLC is recalling 50 kits of Regard TOTAL HIP implants distributed in Missouri due to incorrect product identification labeling on individual kits. This mislabeling could result in the wrong implant being used in surgery.
Organic By Nature, Inc. is recalling Purim Health Brands EpiGenius Kids Chocolate: Daily Superfood pouches due to undeclared milk in an MCT powder ingredient. The product poses a risk to consumers with milk allergies.
Stryker Sustainability Solutions is recalling 40 units of Color Cuff 18" tourniquet cuffs (Lot #12983349) because they are mislabeled as single-bladder when they are actually dual-bladder, creating a risk of incorrect clinical use.
Medline Industries is recalling 494,273 CURAD Reusable Gel Hot/Cold Packs because the product contains natural rubber latex that is not disclosed on the label. Consumers with latex allergies face risk of allergic reaction.
Amy's Kitchen is recalling its Vegan Organic Rice Mac & Cheese due to undeclared milk detected during testing. The product is labeled dairy-free, posing a risk to consumers with milk allergies.
Microbiologics' LYSO Disk culture disks labeled as containing Actinomyces odontolyticus have been found to actually contain Eggerthella lenta. The mislabeling affects products distributed to Canada and Germany.
Microbiologics Inc is recalling KWIK-STIK microorganism reference kits labeled as Actinomyces odontolyticus but containing Eggerthella lenta. The mislabeling could cause incorrect organism identification in laboratory testing.
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling. The recall affects 6,430 cartons distributed throughout the USA.
Beaverton Foods Inc is recalling Inglehoffer Seafood Tartar Sauce with Lemon & Capers because the ingredient label declares soybean oil but does not adequately disclose soy as an allergen, posing a risk to consumers with soy allergies.
Renaissance Food Group is recalling Chicken Salad Croissants because some packages contain Tuna Salad, which is not declared on the label. Fish is a major allergen and poses a serious risk to consumers with fish allergies.
Local Fixe LLC is recalling Classic Lasagna Pasta sheets because the label declares flour as an ingredient but fails to declare wheat, which is present in the product. Consumers with wheat allergies may face serious health risks.
Howling Cow Butter Almond ice cream sold in North Carolina and South Carolina contains Cookie Dough Ice Cream with undeclared soy and wheat allergens. Consumers with allergies should not consume the product.
Cook Inc. is recalling the Flexor Check-Flo Introducer due to mislabeled packaging where 6FR devices may be labeled as 7FR or vice versa. This size mislabeling could result in selection of the wrong device size.
Cook Inc. is recalling Flexor Check-Flo Introducer devices due to mislabeling where packages marked as 6FR may contain 7FR devices, or vice versa. This sizing mismatch could result in improper device selection during clinical vascular procedures.
Intuitive Surgical recalls 1,740 da Vinci Instrument Arm Drapes due to incorrect expiration dates on package labeling. The error may prevent accurate verification of sterility assurance dates.
Picket Fence Creamery is recalling Bacon-Ranch White Cheddar cheese curds due to undeclared soy lecithin. The product may pose a risk to consumers with soy allergies.
Mountain View Bakery is recalling Chocolate Cake Rolls (4oz and 8oz) distributed to Pilot gas stations in Tennessee because the product contains undeclared milk, a common allergen.
Keystone RV Company is recalling 2022 Arcadia fifth wheel travel trailers because the Federal Identification Label contains incorrect tire size and pressure information. This could lead to over-inflation and increase the risk of crashes.
W L Gore & Associates is recalling 187 units of GORE CARDIOFORM Septal Occluders because they are labeled with a 3-year expiration date instead of the correct 2-year expiration date. Using the device beyond its actual shelf life could compromise its safety and effectiveness.
GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.
Limacorporate S.p.A is recalling 151 units of bone screws because the labeled length may not match the actual screw length included in the package.
Angiodynamics is recalling Xcela PICC catheters where units labeled as 5F are actually 4F. The labeling discrepancy between labeled and actual product size could affect clinical device selection.