US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 4, 2016 (10 years ago)

OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx…

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

Why it was recalled

Failed Impuities/Degradation Specifications

What was recalled

OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-04

Recalling firm
Fresenius Kabi USA, LLC
NDC code
63323-365-04
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0867-2016

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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