Class II

Medical Device Recall: Baxter TruSystem 7500, Product Code 4091000

Baxter Healthcare Corporation · February 25, 2025

Reason for Recall

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

1709 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1422-2025

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.