Class II
Terminated
Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-0900-30, UPC 3-0591090030-4
This recall has been terminated (originally issued February 22, 2017).
- Company
- Actavis Inc
- Recall Initiated
- January 30, 2017
- Posted
- February 22, 2017
- Recall Number
- D-0476-2017
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 499320 units
- Firm Location
- Parsippany, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Dissolution Specifications. Above out of specification for dissolution rate observed at the 10 hour testing point.
Distribution
Nationwide in US
Lot / Code Info
Lot #: 3134201, 3134202, Exp. 06/30/17; 3134319, Exp. 05/31/17; 3135246, Exp. 07/31/17; 3135247, 3136781, Exp. 08/31/17; 3136782, Exp. 09/30/17; 3136903, 3136904, Exp.10/31/17; 3138250, Exp. 07/31/17; 3138968, Exp. 08/31/17; 3140000, Exp. 09/30/17
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