Class III
Terminated
Duloxetine Delayed-release Capsules, USP, 60 mg, Rx Only, 1000 count bottle, Manufactured by: Laboratorios Dr. Esteve, S.A., Barcelona, Spain, Distributed by: Breckenridge Pharmaceutical, Inc., Boca Raton, FL 33487, NDC: 51991-748-10
- Company
- Breckenridge Pharmaceutical, Inc
- Recall Initiated
- October 21, 2015
- Posted
- November 18, 2015
- Recall Number
- D-0181-2016
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 595 Bottles
- Firm Location
- Berlin, CT, United States
Reason for Recall
Presence of Foreign Tablets/Capsules: one foreign capsule identified as omeprazole 10 mg was found in the bottle
Distribution
Nationwide
Lot / Code Info
Lot #: 142391, Exp 10/2016
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