Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Lactated Ringer's Injection Recalled by Hospira, Inc. Due to CGMP Deviations: Shipment of product not approved for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hospira, Inc. directly.
Affected Products
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Quantity: 1,296 units
Why Was This Recalled?
CGMP Deviations: Shipment of product not approved for release.
Where Was This Sold?
This product was distributed to 1 state: NC
About Hospira, Inc.
Hospira, Inc. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report