Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter Electrocardiograph Recalled by Baxter Healthcare Corporation Due to One ELI 380 Electrocardiograph intended to be used...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Baxter Electrocardiograph, ELI 380 -DCS21
Quantity: 1 unit
Why Was This Recalled?
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.
Where Was This Sold?
This product was distributed to 1 state: TX
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report