Zoloft recall: Superpotent
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
Why was Zoloft recalled?
SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: S84026
- Product
- 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
- Recalling firm
- Pfizer Inc.
- Quantity
- 1972 bottles
- Distribution
- Nationwide in the USA
- Recall date
- January 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)