FDA recall D-0350-2020
ICU Medical Inc · Class I · drug
Product
0.9% SODIUM CHLORIDE INJECTION, USP, 250 mL VisIV Container, Rx Only, Hospira, Inc. Lake Forest, IL 60045. NDC 0409-7983-25
Reason for recall
Presence of Particulate Matter.
Distribution
Nationwide in the USA.
Key facts
- Status
- Terminated
- Initiation date
- 2019-10-25
- Report date
- 2019-11-13
- Termination date
- 2022-01-20
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Lake Forest, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0350-2020