Complete FDA and NHTSA recall records dated in 2023, 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.
The recalled product did not meet the pre-kill step processing specifications and has the potential to be spoiled.
The manufacturer informed the firm that they received a complaint of plastic in the product.
Corim Industries, 1112 Industrial Parkway, Brick, NJ 08724 is initiating a recall of Agglomerated Peanut Butter Hot Chocolate, Peanut Butter Cappuccino, 500lb sacks; single serve cups…
Dried fish bones were found in product.
Product was found to contain the allergen of soy that was not listed on the ingredient label.
May contain undeclared peanut residue.
May contain undeclared peanut residue.
Corim Industries, 1112 Industrial Parkway, Brick, NJ 08724 is initiating a recall of Agglomerated Peanut Butter Hot Chocolate, Peanut Butter Cappuccino, 500lb sacks; single serve cups…
Ford Motor Company (Ford) is recalling certain 2023 Bronco Wildtrak and 2022 Bronco Raptor vehicles. Internal damage to the steering gear may require increased steering effort or cause the…
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
Lack of Assurance of Sterility
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
CGMP Deviations: recalling drug products following an FDA inspection.
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.
