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Recall Observatory FDA recall evidence

Drug product

Dabigatran Etexilate, 75 mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-474-60

D-0129-2025

December 12, 2024

Class II

Product summary

Firm
Ascend Laboratories, LLC
Event
Event 95896
Status
Ongoing
Classification
Class II
Quantity
1971 bottles
Official record key
drug-enforcement:D-0129-2025

Official wording

Reason: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit

Code information: Lot #: 24142328, 24142329, 24142330, Exp. Date May 31, 2026.

Distribution pattern: Nationwide within the United States

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    N-nitroso-Dabigatran impurity
  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations