Class II
Terminated
Duloxetine Delayed-Release Capsules, USP, 60 mg, Rx Only, 30 Capsules per Bottle, Manufactured in Israel by: Teva Pharmaceutical IND, LTD, Jerusalem, Israel, Manufactured for: Teva Pharmaceuticals USA, Sellersville, PA, 18960, NDC 0093-7544-56
- Company
- Teva Pharmaceuticals Usa
- Recall Initiated
- March 4, 2014
- Posted
- April 9, 2014
- Recall Number
- D-1184-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 324,648 Bottles
- Firm Location
- Horsham, PA, United States
Reason for Recall
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend regarding capsule breakage.
Distribution
Nationwide, Guam, Puerto Rico, American Samoa, Virgin Islands.
Lot / Code Info
Lot #: 50D003, Exp. 2/2015; 50D004, 50D005, Exp. 3/2015; 50D006, Exp. 5/2015; 50D010, Exp. 6/2015; 50D028, Exp. 9/2015; 50D029, 50D031, Exp. 10/2015; 50D032, 50D033, Exp. 11/2015
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