US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 28, 2016 (10 years ago)

Zoloft (sertraline HCl) tablets, 100 mg*, 30 count bottles, Rx only, Distributed by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Tablet/Capsule Specifications: thick tablets exceeding specifications were found.

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.

Recalling firm
Pfizer Inc.
NDC code
0049-4910-30
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0857-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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