Class II
Medical Device Recall: Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886
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
24 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1421-2025
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.