Class II — Baxter Healthcare Corporation
| Recalling firm | BAXTER HEALTHCARE CORPORATION |
|---|---|
| Registered facility | View this company's 32 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display. |
| Product | Welch Allyn Connex Spot Monitor |
| Quantity | 2 units |
| Distribution | US Nationwide distribution in the state of CA. |
| Initiated | 2023-08-10 |
| Classified | 2023-09-12 |
| Recall number | Z-2581-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Baxter Healthcare Corporation (Z-2581-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92874/
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