FDAAugust 16, 2019drug

Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.

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

The hazard

Lack of Assurance of Sterility.

What to do

FDA enforcement status: Terminated

Brands named

sca pharmaceuticalssca

UPCs

70004043009

Recall history

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

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