The Kroger Co Country Oven Party Balloon Cake 48oz recall — FDA F-0154-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Complete FDA and NHTSA recall records dated in 2021, 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.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Product may contain Metronidazole
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Product may contain Metronidazole
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.
Failed Excipient Specification; product manufactured using an excipient found to be OOS for conductivity
cGMP Deviations: Product manufactured with contaminated raw ingredient.
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin…
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.