Baxter Electrocardiograph — Class II medical device recall Z-1013-2023
Terminated recall by Baxter Healthcare Corporation, reported 2023-02-01, distributed in TX. One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on
| Recall number | Z-1013-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-10-31 |
| Classified | 2023-01-24 |
| Reported by FDA | 2023-02-01 |
| Terminated | 2025-03-06 |
| Distributed | TX |
| Quantity | 1 units |
| Lot numbers | 122420001706 |
Product
Baxter Electrocardiograph, ELI 380 -DCS21
Reason for recall
One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1013-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.