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U.S. Department of Health and Human Services

Enforcement Report - Week of August 14, 2013

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Product Detail

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

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
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