Pfizer Inc. recalls Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., NY, NY,…
- Recall date
- October 20, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0151-2018
- FDA classification
- Class II
- Brand / firm
- Pfizer Inc.
- Sold / distributed
- Nationwide in the USA
Why it was recalled
SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., NY, NY, 10017 NDC 0049-4960-30
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