Pfizer Inc. recalls Zoloft (sertraline HCl) tablets, 100 mg*, 30 count bottles, Rx only, Distributed by Roerig, Division of Pfizer, Inc., N…
- Recall date
- April 28, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0857-2016
- FDA classification
- Class II
- Brand / firm
- Pfizer Inc.
- Sold / distributed
- Nationwide and Puerto Rico
Why it was recalled
Failed Tablet/Capsule Specifications: thick tablets exceeding specifications were found.
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, 100 mg*, 30 count bottles, Rx only, Distributed by Roerig, Division of Pfizer, Inc., NY NY 10017, NDC 0049-4910-30.
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