FDA recall Z-0348-2025
Baxter Healthcare Corporation · Class II · device
Product
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Reason for recall
The door on the Spectrum IQ Infusion pump may not be able to fully close.
Distribution
GA, ID
Key facts
- Status
- Ongoing
- Initiation date
- 2024-10-02
- Report date
- 2024-11-20
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Deerfield, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0348-2025