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Recall Observatory FDA recall evidence

Drug product

Accuretic (quinapril HCl/hydrochlorothiazide) Tablets, 20 mg/25 mg, 90 tablets bottles, Rx Only, Distributed by: Parke-Davis, Division of Pfizer Inc, NY, NY 10017, Made in Germany, NDC 0071-0223-23.

D-0757-2022

March 21, 2022

Class II

Product summary

Firm
Pfizer Inc.
Event
Event 89864
Status
Terminated
Classification
Class II
Quantity
265 bottles
Official record key
drug-enforcement:D-0757-2022

Official wording

Reason: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Code information: Lot ET6974; Exp. 02/2023

Distribution pattern: Nationwide

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    N-nitroso-hydrochlorothiazide impurity
  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations