US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 27, 2017 (9 years ago)

Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.

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

Why it was recalled

Lack of sterility assurance.

What was recalled

Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.

Recalling firm
Pharmedium Services, LLC
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0441-2018

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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