Hazard
272 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 class iii 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.
Cajeta cupcakes and other cake products are being recalled because they contain goat milk, which was labeled simply as "milk". 24 units are affected.
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
LION Watermelon Spring Water Hydration Drink in 20 fl oz bottles is being recalled because of potential contamination with floating objects. 48 cases are affected.
LION Pineapple Spring Water Hydration Drink in 20 fl oz bottles is being recalled because of potential contamination with floating objects. 41 cases are affected.
LION Lemon Lime Spring Water Hydration Drink in 20 fl oz bottles is being recalled because of potential contamination with floating objects. 58 cases are affected.
New Mexico Pinon Coffee Dark Pinon Single Serve cups are being recalled because an inconsistent clear coat seal allows the food safe ink printing to run in a K-cup machine. 154 units affected.
LION Mixed Berry Spring Water Hydration Drink in 20 fl oz bottles is being recalled because of potential contamination with floating objects. 43 cases are affected.
Pasteurized Donor Human Milk in 4 oz bottles is being recalled because plastic particulate from the outer closure was found between the foil seal and the plastic cap. 209 bottles are affected.
Boar's Head Smoked Gouda in 8 oz packages is being recalled because of mislabeling. 65 cases are affected, distributed in Florida.
Compounded Testosterone 200 mg Pellet in 1 mL amber vials is being recalled because a printing issue resulted in incorrect lot numbers on the label. 2,832 vials are affected.
Calais brand Grape Jelly in 1 gallon containers is being recalled because it contains undeclared colours FD&C Blue 1 and FD&C Red 40. 43 cases are affected.
Shoppers Value Fruit Cocktail in heavy syrup is being recalled because of undeclared Red No. 3 (E127). 1,105 cases are affected.
Daniele brand First Cold Press Extra Virgin Olive Oil in 3 L containers is being recalled because the product is likely canola oil, not extra virgin olive oil. 10 cases are affected.
TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.
TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.
TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.
TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.
TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.
Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.
Pitavastatin Tablets 1 mg manufactured by Orient Pharma for Teva Pharmaceuticals are being recalled because they failed impurities and degradation specifications. 20,618 bottles affected.
Pitavastatin Tablets 1 mg from AvKARE are being recalled because they failed impurity and degradation specifications. 1,560 bottles are affected.
Eight Valeda Light Delivery Systems are being recalled because US customers were shipped devices configured for the European Union that could not be plugged into the outlet.