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U.S. Department of Health and Human Services

Enforcement Report - Week of August 14, 2013

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Event Detail

Event ID 64792
Product Type Drugs
Status Ongoing
Recalling Firm Hospira Inc.
City Lake Forest
State IL
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-03-29
Initial Firm Notification of
Consignee or Public
Press Release
Distribution Pattern Nationwide

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09. Lot #: 25-037-JT*, Exp 1JAN2015, Note: the lot number may be followed by 01 or 90 Class I Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates 691,356 containers D-836-2013
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