VERMOX Tablets 100 mg recalled over manufacturing violations
- Recall date
- May 11, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Profarma Distributors LLC recalls VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
- Recall number
- D-1041-2016
- FDA classification
- Class II
- Brand / firm
- Profarma Distributors LLC
- Sold / distributed
- Nationwide
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
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