Complete FDA and NHTSA recall records dated in 2014, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Products contain eggs which were recalled due to susceptibility to premature spoilage.
Products contain eggs which were recalled due to susceptibility to premature spoilage.
Lotte International is recalling the Lotte Waffles because it contains undeclared eggs.
The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.
BBM Chocolate Distributors, Ltd. has recalled three (3) Alprose Dark Chocolate products due to the presence of undeclared milk allergen.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Increased number of complaints that product is not softening as intended and causes a potential choking hazard in babies and young children,.
Product may be contaminated with spoilage microorganism.
Products contain eggs which were recalled due to susceptibility to premature spoilage.
Products contain eggs which were recalled due to susceptibility to premature spoilage.
Products were recalled due to potential Listeria monocytogenes contamination.
This voluntary recall has been initiated because the Kupiec Rice Cakes with Dark Chocolate may contain undeclared milk.
The firm was notified by the Ohio Department of Agriculture that Sassafras Leaves may be an illegal ingredient for their product.
BBM Chocolate Distributors, Ltd. has recalled three (3) Alprose Dark Chocolate products due to the presence of undeclared milk allergen.
Glaser Organic Farms has been notified by its supplier Earth Circle Organics, of a recall of Organic Carob Powder due to possible health risks related to Salmonella contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Superpotent Drug: Bio-Pharm, Inc. is initiating a recall of one lot of Acetaminophen Oral Suspension Liquid 160mg/5mL failure of the product assay at the 6 month timepoint.
Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three flavors of Acetaminophen Oral Suspension Liquid 160mg/5mL for failure of the product assay at the 12 month…
Subpotent Drug: Product failed to meet USP Specifications on assay, content uniformity, and dissolution.
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not Approved for…
Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not Approved for…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
