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Recall Observatory FDA recall evidence

Drug product

Tranexamic Acid Injection, USP, 1000 mg/10 mL (100 mg/mL), 10 mL Single-Dose Vial (NDC 67457-197-00); 10 x 10 mL Single-Dose Vials per carton (NDC 67457-197-10), Rx only, Manufactured by: Mylan Institutional, Galway, Ireland; Manufactured for: Mylan Institutional LLC, Rockford, IL 61103.

D-1576-2020

August 17, 2020

Class I

Product summary

Firm
Mylan Institutional LLC
Event
Event 86247
Status
Terminated
Classification
Class I
Quantity
1407 cartons
Official record key
drug-enforcement:D-1576-2020

Official wording

Reason: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled as Amiodarone HCl Injection, USP to contain vials of Tranexamic Acid Injection, USP.

Code information: Lot #: 191207, 191221, 191223, Exp. 11/2021; 200120 Exp. 12/2021

Distribution pattern: Nationwide

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Labeling: Label Mix-Up