FDA Device recall Z-2581-2023
Welch Allyn Connex Spot Monitor
- FDA Device
- Class II
- ongoing
- Published 2023-09-20
On 2023-09-20 the FDA classified a Class II recall of Welch Allyn Connex Spot Monitor by Baxter Healthcare, citing product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2581-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-10 |
| Published | 2023-09-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Welch Allyn Connex Spot Monitor
Reason
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
Identifiers
| code_info | Product Code: 75MT-B; UDI: 00732094209372; Serial Numbers: 100027582923 and 100027862923 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2581-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.