FDA recall D-215-2013
Hospira, Inc. · Class III · drug
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.
Distribution
NC
Key facts
- Status
- Terminated
- Initiation date
- 2012-06-21
- Report date
- 2013-04-03
- Termination date
- 2013-03-28
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Lake Forest, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-215-2013