FDAFDA · Food and drugs·Recall number D-0010-2019
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
Published October 17, 2018 · Recall initiated: September 20, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations; rejected product was used to manufacture final bulk lot
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide
- Lot
- Lot: T71137 Exp. Feb. 2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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