Teva Pharmaceuticals USA recalls Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA…
- Recall date
- July 24, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1056-2017
- FDA classification
- Class II
- Brand / firm
- Teva Pharmaceuticals USA
- Sold / distributed
- Nationwide
Why it was recalled
Failed Tablet/Capsule Specification; out of specification for tablet weight
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
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