Class II

Medical Device Recall: Spectrum IQ Infusion pump, Product Code 357009

Baxter Healthcare Corporation · April 9, 2024

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.

States Affected

NATIONWIDE

Quantity Affected

9 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1810-2024

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.