FDA recall D-1226-2014

Hospira Inc. · Class III · drug

Product

Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.

Reason for recall

Labeling; Missing label; ampoules are missing the immediate container label

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2014-03-25
Report date: 2014-04-16
Termination date: 2015-12-18
Voluntary/Mandated: Voluntary: Firm initiated
Location: Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1226-2014