US Drug Recall Register
Class I · High risk Terminated Initiated Apr 17, 2012 (14 years ago)

Morphine Sulfate Injection, USP, 4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Superpotent; Cartridges labeled to contain 1 mL found to contain 2.2 mL

What was recalled

Morphine Sulfate Injection, USP, 4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, Hospira, Inc., Lake Forest, IL ---- NDC 0409-1258-30

Recalling firm
Hospira Inc.
NDC code
0409-1258-30
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1419-2012

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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