Lactated Ringer's Injection recall: CGMP Deviations
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Why was Lactated Ringer's Injection recalled?
CGMP Deviations: Shipment of product not approved for release.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 16-836-FW, Exp 04/14
- Product
- Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
- Recalling firm
- Hospira, Inc.
- Quantity
- 1,296 units
- Distribution
- NC
- Recall date
- April 3, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)