Drug Enforcement D-922-2013

Presence of Particulate Matter; product may contain fibrous material

Status

Terminated

Classification

Class I

Report Date

September 4, 2013

Termination Date

May 28, 2015

Product Information

Product description
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Product quantity
264,432 bags
Reason for recall
Presence of Particulate Matter; product may contain fibrous material
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-922-2013
Event ID
63364
Recall initiation date
August 31, 2012
Center classification date
August 26, 2013
Code info
Lot Number 05-201-JT, Expiration Date 1MAY2013
More code info