Class II
Terminated
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
- Company
- Pfizer Inc.
- Recall Initiated
- September 20, 2018
- Posted
- October 17, 2018
- Recall Number
- D-0010-2019
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 7777 bottles
- Firm Location
- New York, NY, United States
Reason for Recall
CGMP Deviations; rejected product was used to manufacture final bulk lot
Distribution
Nationwide
Lot / Code Info
Lot: T71137 Exp. Feb. 2022
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