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Baxter Healthcare Corporation recalls GEM FLOW COUPLER Monitor, PN 5156-00000-011
Recalled July 26, 2023 · FDA recall Z-2208-2023 · Baxter Healthcare
Hazard
An issue was identified where the LCD monitor display may not indicate the correct active channel. The issue occurs when the monitor is turned on using battery power, and channel B was selected as the last active channel prior to powering down. · FDA Class II
Units
122 units
Sold at
US
Description
An issue was identified where the LCD monitor display may not indicate the correct active channel. The issue occurs when the monitor is turned on using battery power, and channel B was selected as the last active channel prior to powering down.
Product
GEM FLOW COUPLER Monitor, PN 5156-00000-011
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →