FDAClass IISeptember 20, 2017

Paroxetine tablets USP recall

Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8

Why was Paroxetine tablets USP recalled?

Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets

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 #: Z701133, Exp 03/19

Product
Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8
Recalling firm
Zydus Pharmaceuticals USA Inc
Quantity
44800 bottles
Distribution
Nationwide within United States
Recall date
September 20, 2017
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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