Class II
Medical Device Recall: Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one unit per carton Component: N/A
Baxter Healthcare Corporation · January 13, 2026
Reason for Recall
Pumps were released without full testing being performed, including occlusion alarm testing.
Distribution
States: Ohio Countries: United States
Quantity Affected
5
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1368-2026
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.