FDAOctober 31, 2022device

Baxter Electrocardiograph, ELI 380 -DCS21

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

UPCs

122420001706

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Baxter Electrocardiograph, ELI 380 -DCS21 — Recall Details · AllClear