Class II
Terminated
quinapril and hydrochlorothiazide tablets, 20 mg/25 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-5225-9
- Company
- Pfizer Inc.
- Recall Initiated
- March 21, 2022
- Posted
- April 13, 2022
- Recall Number
- D-0758-2022
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 2442 bottles
- Firm Location
- New York, NY, United States
Reason for Recall
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Distribution
Nationwide
Lot / Code Info
Lot FE3714; Exp. 02/2023
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