FDA recall D-922-2013
Hospira Inc. · Class I · drug
Product
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Reason for recall
Presence of Particulate Matter; product may contain fibrous material
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2012-08-31
- Report date
- 2013-09-04
- Termination date
- 2015-05-28
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Lake Forest, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-922-2013