FDA recall Z-1775-2024
Baxter Healthcare Corporation · Class II · device
Product
Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Reason for recall
One device was improperly performed testing prior to release from a Service Center.
Distribution
US Nationwide distribution in the state of Massachusetts.
Key facts
- Status
- Ongoing
- Initiation date
- 2024-03-20
- Report date
- 2024-05-15
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Deerfield, IL, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1775-2024