January 2013 FDA Recall Drug by Teva Pharmaceuticals Usa, Inc.
D-193-2013 - Presence of Foreign Tablets/Capsules

This Class II drug recall was voluntarily initiated by Teva Pharmaceuticals Usa, Inc. on January 23, 2013 for the product Drug. 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-193-2013

Reason for Recall
Presence of Foreign Tablets/Capsules: Recall is being conducted due to a foreign capsule found in one bottle.
Initiated
01-23-2013
Reported
03-20-2013
Quantity
3,913 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
Teva Pharmaceuticals USA, Inc.
Terazosin Hydrochloride Capsules, 2 mg, packaged in a) 100-count bottles (NDC 0093-4337-01); and b) 1000-count bottles (NDC 0093-4337-10), Rx only, Manufactured in India By: Intas Pharmaceuticals Ltd., Ahmedabad, Gujarat, India - 382 210; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960.

Batch or Lot Expiration Information

Lot# N03029, Exp 03/14