FDA recall D-0883-2018
ICU Medical Inc · Class II · drug
Product
0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-23
Reason for recall
Lack of assurance of sterility: Bags have potential to leak.
Distribution
Nationwide and Canada
Key facts
- Status
- Terminated
- Initiation date
- 2018-05-31
- Report date
- 2018-06-27
- Termination date
- 2020-06-04
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- LAKE FOREST, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0883-2018