FDAFDA · Food and drugs·Recall number D-0151-2018
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
Published January 10, 2018 · Recall initiated: October 20, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the USA
- Lot
- Lot: S84026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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