US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 24, 2013 (13 years ago)

Oxytocin Injection, USP, (Synthetic), 10 USP Units/mL, for IV Infusion or IM Use, Rx…

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

Why it was recalled

Subpotent Drug; 15-month stability test station

What was recalled

Oxytocin Injection, USP, (Synthetic), 10 USP Units/mL, for IV Infusion or IM Use, Rx Only, 1 mL vial, APP ) 10 USP Units/mL, 1 mL, APP Pharmaceuticals, LLC Schaumburg, IL, 60173, NDC 63323-012-01.

Recalling firm
Fresenius Kabi USA, LLC
NDC code
63323-012-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-804-2013

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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