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Recall Observatory FDA recall evidence

Drug product

Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-558-09

D-0089-2023

December 07, 2022

Class II

Product summary

Firm
Lupin Pharmaceuticals Inc.
Event
Event 91279
Status
Terminated
Classification
Class II
Quantity
23,736
Official record key
drug-enforcement:D-0089-2023

Official wording

Reason: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

Code information: Lot #: G102929, Exp 04/2023

Distribution pattern: Product was distributed by major distribution chains nationwide.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    N-Nitroso-quinapril impurity
  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations