RecallDepth
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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