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.
Products with a gluten free claim may contain gluten levels above 20 ppm.
Products with a gluten free claim may contain gluten levels above 20 ppm.
This recall has been initiated because a contamination event downstream of the thermal process deemed the product not commercially sterile and creates the potential for product spoilage.
Potential soft rubber fragments in the product, which could pose the risk of a choking hazard.
Undeclared sesame in cookies
Products with a gluten free claim may contain gluten levels above 20 ppm.
This recall has been initiated because a contamination event downstream of the thermal process deemed the product not commercially sterile and creates the potential for product spoilage.
Possible risk of pathogen contamination due to inadequate pasteurization.
Products with a gluten free claim may contain gluten levels above 20 ppm.
Potential undeclared allergen from cross contamination. Product contains tree nuts (hazelnuts and walnuts) and potential cross contamination from other tree nuts (almonds and cashews).
Product was not stored refrigerated.
Products with a gluten free claim may contain gluten levels above 20 ppm.
Sesame is declared in the Ingredients statement but it is not declared in the Contains statement.
Undeclared sesame in cookies
Potential undeclared allergen from cross contamination. Product contains tree nuts (hazelnuts and walnuts) and potential cross contamination from other tree nuts (almonds and cashews).
CGMP deviation: product outside labeled storage temperature requirements.
Superpotent Drug and Failed Impurities/Degradation Products: formula does not adhere to the labeled specifications
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of…
CGMP deviation: product outside labeled storage temperature requirements.
Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive…
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of…
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of…
CGMP deviation: product outside labeled storage temperature requirements.
Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or…
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.
