FDA recall D-1234-2014

Hospira, Inc. · Class I · drug

Product

1% Lidocaine HCl Injection, USP, 10 mg/mL, NDC 0409-4276-01, Hospira, Inc., Lake Forest, IL 60045.

Reason for recall

Presence of Particulate Matter: Oxidized stainless steel found in vial of 1% Lidocaine Hydrochloride Injection, USP.

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2013-09-16
Report date: 2014-04-23
Termination date: 2014-11-04
Voluntary/Mandated: Voluntary: Firm initiated
Location: Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1234-2014