Gericare Geri-Tussin DM recalled over manufacturing violations
- Recall date
- May 31, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Geritrex, LLC recalls Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660…
- Recall number
- D-1526-2019
- FDA classification
- Class II
- Brand / firm
- Geritrex, LLC
- Sold / distributed
- U.S.A. Nationwide
Why it was recalled
cGMP Deviations: Products may have microbial contamination.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16
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