Medical Device Recall: Spectrum IQ Infusion Pump, Product Code 3570009
Baxter Healthcare Corporation · July 14, 2025
Reason for Recall
Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.
Distribution
US distribution to states of: AZ, FL
States Affected
AZ, FL
Quantity Affected
6 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2415-2025
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.