August 2017 FDA Recall Paroxetine by Zydus Pharmaceuticals Usa Inc
D-1137-2017 - Presence of Foreign tablets/capsules

This Class II drug recall was voluntarily initiated by Zydus Pharmaceuticals Usa Inc on August 18, 2017 for the product Paroxetine. The FDA reported the reason for recall as presence of foreign tablets/capsules. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1137-2017

Reason for Recall
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Initiated
08-18-2017
Reported
09-20-2017
Quantity
44800 bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Zydus Pharmaceuticals USA Inc
Nationwide within United States
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

Batch or Lot Expiration Information

Lot# : Z701133, Exp 03/19