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Recall Observatory FDA recall evidence

Drug product

Amikacin Sulfate Injection, USP, 1 gm/4 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-9040-01 (individual pack), NDC 0703-9040-03 (shelf-pack carton of 10 vials).

D-0024-2017

July 29, 2016

Class II

Product summary

Firm
Teva Pharmaceuticals USA
Event
Event 74816
Status
Terminated
Classification
Class II
Quantity
11,844 vials
Official record key
drug-enforcement:D-0024-2017

Official wording

Reason: CGMP Deviations

Code information: Lot # 2381114, 2771114, 4760915

Distribution pattern: Nationwide and Puerto Rico

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations