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U.S. Department of Health and Human Services

Enforcement Report - Week of April 3, 2013

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Product Detail

Product Description Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Recall Number D-215-2013
Classification Class III
Code Info Lot 16-836-FW, Exp 04/14
Product Distributed Qty 1,296 units
Reason For Recall CGMP Deviations: Shipment of product not approved for release.

Event Detail

Event Id 63242
Product Type Drugs
Status Terminated
Recalling Firm Hospira, Inc.
City Lake Forest
State IL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-06-21
Initial Firm Notification of Consignee or Public Telephone
Distribution Pattern NC