PlainRecalls
FDA Drug Low Class III Terminated

Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09

Reported: April 3, 2013 Initiated: June 21, 2012 #D-215-2013

Product Description

Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09

Reason for Recall

CGMP Deviations: Shipment of product not approved for release.

Details

Recalling Firm
Hospira, Inc.
Units Affected
1,296 units
Distribution
NC
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09. Recalled by Hospira, Inc.. Units affected: 1,296 units.
Why was this product recalled?
CGMP Deviations: Shipment of product not approved for release.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 3, 2013. Severity: Low. Recall number: D-215-2013.