Class II
Medical Device Recall: Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2
Baxter Healthcare Corporation · June 14, 2024
Reason for Recall
Improperly performed testing prior to release
Distribution
US Nationwide distribution in the state of Florida.
States Affected
NATIONWIDE
Quantity Affected
1 unit
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2530-2024
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.