Class II
Medical Device Recall: Baxter Spectrum IQ Infusion Pump, Product Code 3570009
Baxter Healthcare Corporation · March 20, 2024
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.
States Affected
NATIONWIDE
Quantity Affected
1 pump
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1775-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.