Baxter Healthcare Corporation Baxter Electrocardiograph, ELI 380 -DCS21 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Electrocardiograph, ELI 380 -DCS21
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
Lot number 122420001706
Products Sold
Lot number 122420001706
Baxter Healthcare Corporation is recalling Baxter Electrocardiograph, ELI 380 -DCS21 due to One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.
Recommended Action
Per FDA guidance
The customer was contacted on 31 October 2022 to inform them of the issue and instructed not to install the device for use.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
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Page updated: Jan 10, 2026