Hazard
9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 9,606 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) 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 mis labeling 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.
Frickenschmidt Foods LLC is recalling ready-to-eat teriyaki beef sticks because they are labeled 'gluten free' but contain wheat. No adverse reactions have been reported.
Lily's Sweets is recalling 7 oz. pouches of Peppermint Flavor Baking Chips because they contain undeclared soy lecithin, a common allergen. The product was distributed to 22 U.S. states.
Great American Cobbler LLC is recalling Creole Style Chicken Pot Pie products because they contain soy, a known allergen, that is not declared on the label.
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because the gross vehicle weight rating may be incorrectly stated on the tire and loading label.
YOUNG DH Dry Heat Indicator Labels used in healthcare sterilization may contain TTS Indicator Labels instead. Healthcare providers should verify package contents before use to ensure proper sterilization monitoring.
Microbiologics Inc is recalling KWIK-STI(TM) GBS QC Set components with a mislabeled expiration date. The Lactobacillus acidophilus component was labeled 7/31/2020 instead of 7/31/2022.
Olympus Corporation is recalling 35 units of the Spiration Valve System (SVS-V9-00) due to a mislabeled patient charge label indicating model SVS-V7-00 instead. The incorrect label could confuse healthcare providers about which valve was implanted.
Celltrion USA Inc. is recalling 162,000 units of the European version of its DiaTrust COVID-19 Ag Rapid Test, which was not approved for U.S. distribution. The test packaging and labeling differ from the FDA-approved U.S. version.
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling on certain cartons. The recall affects 218,174 cartons distributed in the United States.
Dental Alliance Holdings LLC is recalling the CTx36 Kit because it contains less sodium fluoride than stated on the product label. Affected patients should contact their dentist.
Beaverton Foods Inc is recalling Beaver Brand Tartar Sauce with Fresh Capers and Dill because soybean oil, a soy derivative, is not declared in the ingredients statement. This product may pose a risk to consumers with soy allergies.
Dental Alliance Holdings LLC is recalling CariFree CTx4 Gel 5000 fluoride gel tubes because they contain less sodium fluoride than stated on the label. The affected product is CTx12 5000 Kit lot 142017.
The FDA is recalling CTx7 Kits distributed nationwide because the product contains less sodium fluoride than stated on the label.
CariFree CTx4 GEL 5000 (Lot 142017) contains less sodium fluoride than stated on the label. The product is being recalled and consumers should contact their healthcare provider with questions.
Straumann USA LLC is recalling certain Neodent Easypack dental implant kits due to mislabeling where packaging does not match the implant dimensions inside. Affected units contain 3.5x8mm implants instead of the labeled 3.5x13mm size.
Philips North America recalls Cardinal Infant Heel Warmers because labeling was changed without FDA approval. The devices cannot be sold or distributed without new FDA clearance.
Straumann USA LLC recalls Neodent Easypack Helix GM Acqua dental implants due to mislabeling. Implants have incorrect dimensions compared to carton labels, which could affect surgical planning and placement.
Philips is recalling 141,750 Infa-Therm Transport Mattresses because modified labeling does not comply with FDA clearance requirements. The devices cannot be distributed or sold without new FDA clearance.
NutraCap Labs LLC is recalling Live Oak Nutrition Alpha Consciousness Capsules (90ct, UPC 7 48528 53969 4) because they contain undeclared milk, a common allergen that poses a risk to consumers with milk allergies.
NutraCap Labs is recalling Soul Nutrition Anxiety unlabeled capsules (90ct bottles, Lot #2109025, expiration 09/2023) because the product contains undeclared milk, a common allergen. The recall affects approximately 80,169 units distributed across 25 states.
NutraCap Labs LLC is recalling UXO Supplements Ghillie Peach Mango 19oz jars because they contain undeclared milk, a common allergen. The product was distributed across 25 states.
NutraCap Labs LLC is recalling ANTLS Supps Turmeric Capsules (120ct) because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.
NutraCap Labs LLC is recalling NatFit Joint Support Capsules 90ct bottles because the product contains undeclared shellfish. Consumers with shellfish allergies who consume the product face a risk of allergic reaction.
NutraCap Labs LLC is recalling DL NutriZone Genone Brain Waves Capsules (120ct bottles) because the product contains undeclared milk, a common allergen. The recall affects approximately 80,169 units distributed across 26 states.
Mass Nutraceuticals Brain Food Capsules are being recalled because they contain undeclared milk. The product was distributed across 25 states and may pose a risk to consumers with milk allergies.