Home / Recalls / Medical Devices
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886
Recalled April 2, 2025 · FDA recall Z-1421-2025 · Baxter Healthcare
Hazard
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled. · FDA Class II
Units
24 units
Sold at
US Nationwide distribution.
Description
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
Product
Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →