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

FDA recall notice · announced April 3, 2013 · Hospira

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

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.

Notes

Distribution: NC
Lot/code information: Lot 16-836-FW, Exp 04/14
Quantity: 1,296 units
Status: Terminated
Products in this recall event:
- Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09 (D-215-2013)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.