FDAJanuary 14, 2020drug

methylPREDNISolone Sodium Succinate For Injection, USP, 500 mg*/vial, Rx Only, Mfd by: HIKMA FARMACEUTICA (PORTUGAL), SA; Dist by: WEST-WARD, Eatontown, NJ 07724, NDC 0143-9850-01.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.

What to do

FDA enforcement status: Terminated

Brands named

hikma pharmaceuticalshikma

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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