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U.S. Department of Health and Human Services

Enforcement Report - Week of September 4, 2013

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Product Detail

Product Description 0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Recall Number D-922-2013
Classification Class I
Code Info Lot Number 05-201-JT, Expiration Date 1MAY2013
Product Distributed Qty 264,432 bags
Reason For Recall Presence of Particulate Matter; product may contain fibrous material

Event Detail

Event Id 63364
Product Type Drugs
Status Ongoing
Recalling Firm Hospira Inc.
City Lake Forest
State IL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-08-31
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide
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