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Baxter Healthcare Corporation recalls Baxter Electrocardiograph, ELI 380 -DCS21
Recalled February 1, 2023 · FDA recall Z-1013-2023 · Baxter Healthcare
Hazard
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022. · FDA Class II
Units
1 unit
Sold at
TX
Description
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.
Product
Baxter Electrocardiograph, ELI 380 -DCS21
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →