FDAFDA · Food and drugs·Recall number D-215-2013
Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
Published April 3, 2013 · Recall initiated: June 21, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: Shipment of product not approved for release.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Hospira, Inc.
- Distributor
- NC
- Lot
- Lot 16-836-FW, Exp 04/14
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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