Welch Allyn Connex Spot Monitor — Class II medical device recall Z-2581-2023
Ongoing recall by Baxter Healthcare Corporation, reported 2023-09-20, distributed nationwide. Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal dis
| Recall number | Z-2581-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2023-08-10 |
| Classified | 2023-09-12 |
| Reported by FDA | 2023-09-20 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 00100027862923, 00732094209372 |
| Serial numbers | 100027582923, 100027862923 |
Product
Welch Allyn Connex Spot Monitor
Reason for recall
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
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-2581-2023. 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.