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Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
Recalled April 2, 2025 · FDA recall Z-1416-2025 · 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
2 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 (MC), Product Code 1773204
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →