FDA recall Z-1810-2024
Baxter Healthcare Corporation · Class II · device
Product
Spectrum IQ Infusion pump, Product Code 357009
Reason for recall
There is a potential for cracks on the mount of the front panel of the device.
Distribution
US Nationwide distribution in the states of Ohio, Wisconsin.
Key facts
- Status
- Ongoing
- Initiation date
- 2024-04-09
- Report date
- 2024-05-22
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Deerfield, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1810-2024