Hazard
1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
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.
A lot of Tornier surgical screws is labeled as 5.0mm x 18mm but actually measures 5.0mm x 14mm. If undetected during surgery, the incorrect screw could increase the risk of mechanical failure and require revision surgery.
Prima Foods International is recalling BarbaCuban 455 Everything Sauce (Hot) due to undeclared quinine. The recall affects bottles distributed in Florida with lot codes #190/24 and #339/24.
Spicely organic sumac is recalled because the product contains salt as an ingredient but displays 'NO SALT' claims on the packaging. 980 cases distributed across 13 U.S. states.
Organic Spices, Inc. is recalling spicely Organic garlic salt because the product contains salt but is labeled as salt-free. The affected product was distributed across 13 U.S. states.
OptiWize Inc. is recalling OptiWize Collagen Plus supplements after NSF testing found that the manganese level did not match what was stated on the label.
Greenstone LLC is recalling methylprednisolone 4 mg tablets due to incorrect blister foil orientation that causes incorrect dosing directions on the packaging.
Haleon is recalling Parodontax mouthwash due to missing or illegible lot and expiration date coding on bottles. Approximately 84,764 bottles were distributed nationwide.
Bazic Products is recalling Bazic Silicone Glue due to methanol poisoning risk. The packaging is not child-resistant as required by law, and the product is incorrectly labeled as non-toxic.
The Leaseir MHR Xcell surgical laser is missing a required 'DANGER' symbol on its console label. This labeling deficiency may prevent operators from being adequately warned of the device's hazards.
CATAO MARKET LLC is recalling Gacen¿iga Authentic Cuban Loaf Cake (24 oz) due to undeclared FD&C Yellow #5. The product was distributed in Florida with Best By dates from 12/18/2025 through 03/18/2026.
Fran's Chocolates Ltd is recalling PureBar Almondmilk Chocolate 46% Madagascar bars (1.1 oz) due to undeclared hazelnut allergen. The product was distributed in Colorado, Massachusetts, Nevada, Washington, and online.
Ukrop's 6" pound cakes are recalled because the label does not disclose soy, though soy is used in the product. Consumers with soy allergies should avoid this product.
House Of Flavors, Inc. is recalling certain 3-gallon containers of 1972 Banana Pudding Ice Cream due to undeclared soy lecithin, a major allergen not listed on the label.
ASK Foods Inc is recalling Publix Rice & Pigeon Peas due to undeclared soy allergen. A total of 2,078 units were distributed to Florida. Consumers with soy allergies should not consume this product.
Ziyad Brothers Importing is recalling Baraka Gourmet Pastry Kunafe 6.7 oz. (UPC 822514291060) because the product may contain partially hydrogenated oils. No illnesses have been reported.
SpecGx LLC is recalling 287,988 bottles of oxycodone and acetaminophen combination tablets due to a potential for missing imprints on some tablets. Affected lot numbers expire from May to June 2027.
A New Life Herbs is recalling Boswellia herbal supplement due to unapproved drug claims on the label and a missing Supplement Facts label.
Mondelez Global is recalling Ritz Peanut Butter Cracker Sandwiches because some packages contain peanuts but lack the required allergen labeling. The recall affects 70 cases distributed to eight states.
A New Life Herbs recalls Anti-virus Herbal Supplement due to unapproved antiviral claims and missing Supplement Facts label. 116 bottles were distributed across 12 states.
A New Life Herbs' Baby Allergy Herbal Supplement is recalled due to unapproved drug claims on the labeling and absence of a required Supplement Facts label. The recall affects 23 bottles distributed across 12 states.
A New Life Herbs is recalling 22 bottles of Mullein flower alcohol tincture ear drops for making unapproved drug claims and lacking required Supplement Facts labeling.
Rocket Medical Plc is recalling Rocket 16Fg Seldinger Catheter Procedure Trays because labeling contains misleading statements that may lead to improper device securing, creating a risk it may fall out during use.
Rocket Medical is recalling the Rocket 12Fg Seldinger Catheter with Safety Guard due to misleading labeling in device kit instructions that may result in improper securing and potential device dislodgement.
Rocket Medical is recalling its 18Fg Seldinger Catheter Procedure Tray due to misleading instructions in device labeling that could lead to improper securing and potential device displacement.
Rocket Medical is recalling the Rocket 12Fg Seldinger Catheter Procedure Tray (635 units) due to misleading labeling that may cause improper securing of the chest tube, risking device fall-out during use.