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
Reported: January 10, 2018 Initiated: October 20, 2017 #D-0151-2018
Product Description
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
Reason for Recall
SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 1972 bottles
- Distribution
- Nationwide in the USA
- Location
- New York, NY
Frequently Asked Questions
What product 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. Recalled by Pfizer Inc.. Units affected: 1972 bottles.
Why was this product recalled? ▼
SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 10, 2018. Severity: Moderate. Recall number: D-0151-2018.
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