US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 17, 2021 (5 years ago)

Morphine Sulfate Injection, USP, 2 mg per mL, 1 mL single dose vial, Rx only, Fresenius…

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

Why it was recalled

Defective container: Cracked vials leading to lack of sterility assurance

What was recalled

Morphine Sulfate Injection, USP, 2 mg per mL, 1 mL single dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-452-01. 25 vials per tray packaged 18 trays per shipper

Recalling firm
Fresenius Kabi USA LLC
NDC code
63323-452-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0856-2021

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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