FDA recall D-1419-2012

Hospira Inc. · Class I · drug

Product

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

Reason for recall

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

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2012-04-17
Report date: 2012-07-25
Termination date: 2015-05-29
Voluntary/Mandated: Voluntary: Firm initiated
Location: Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1419-2012