Tova Industries Shaver Foods brand Frosting Mix Chocolate Texas, Item #32637 recall — FDA F-0802-2020
Downstream recall from supplier. Possible metal shavings in ingredient.
Complete FDA and NHTSA recall records dated in 2020, organized for browsing by month, category and recalling company.
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Records are ordered by the best available source date.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
The firm was notified that the product contains undeclared soy.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Downstream recall from supplier. Possible metal shavings in ingredient.
Possible foreign material.
Product mislabeled as "GF" for gluten-free; however, ingredient statement lists wheat flour as a sub ingredient.
Product may contain undeclared milk allergens in amounts that exceed thresholds established by the New York State Department of Agriculture and Markets.
Failed Content Uniformity Specifications: Out Of Specification test results observed for content and blend uniformity.
Failed Content Uniformity Specifications: Out Of Specification test results observed for content uniformity.
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count…
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
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.