Drug Enforcement D-66201-001

Presence of Particulate Matter; report of visible particulates in the glass ampule

Status

Terminated

Classification

Class II

Report Date

October 9, 2013

Termination Date

November 10, 2014

Product Information

Product description
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
Product quantity
86,400 ampuls
Reason for recall
Presence of Particulate Matter; report of visible particulates in the glass ampule
Recall initiation reason
—
Initial firm notification
Letter
Distribution pattern
Nationwide

Location & Firm

Recalling firm
Hospira Inc.
Address
275 N Field Dr

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date
—

Codes & Dates

Recall number
D-66201-001
Event ID
66201
Recall initiation date
August 29, 2013
Center classification date
October 2, 2013
Code info
Lot 23-227-DK
More code info
—