US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 16, 2019 (7 years ago)

Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration =…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility.

What was recalled

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.

Recalling firm
SCA Pharmaceuticals, LLC
NDC code
70004-0430-09
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1843-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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