Pfizer Inc. recalls Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapac
Recalled October 17, 2018 · FDA recall D-0010-2019 · Pfizer
Hazard
CGMP Deviations; rejected product was used to manufacture final bulk lot · FDA Class II
Units
7777 bottles
Sold at
Nationwide
Description
CGMP Deviations; rejected product was used to manufacture final bulk lot
Product
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →