FDA Device recall Z-1563-2025
Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B by Baxter Healthcare, citing undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1563-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-03-21 |
| Published | 2025-04-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74CX-B; 5) 74ME-B; 6) 74MT-B; 7) 74MX-B; 8) 74RE-B; 9) 74RT-B; 10) 75CE-B; 11) 75CT-B; 12) 75CT-BR; 13) 75CX-B; 14) 75-HCA-CTB; 15) 75-HCA-MTB; 16) 75ME-B; 17) 75MT-B; 18) 75MT-BR; 19) 75MX-B; 20) 75RE-B; 21) 75RT-B; 22) 75WE-B; 23) 75WT-B.
Reason
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Identifiers
| code_info | 1) Product Code/Part # 73WT-B, UDI/DI 00732094210033; 2) Product Code/Part # 74CE-B, UDI/DI 00732094209921; 3) Produc…1) Product Code/Part # 73WT-B, UDI/DI 00732094210033; 2) Product Code/Part # 74CE-B, UDI/DI 00732094209921; 3) Product Code/Part # 74CT-B, UDI/DI 00732094209860; 4) Product Code/Part # 74CX-B, UDI/DI 00732094209792; 5) Product Code/Part # 74ME-B, UDI/DI 00732094209716; 6) Product Code/Part # 74MT-B, UDI/DI 00732094209679; 7) Product Code/Part # 74MX-B, UDI/DI 00732094209624; 8) Product Code/Part # 74RE-B, UDI/DI 00732094335781; 9) Product Code/Part # 74RT-B, UDI/DI 00732094335712; 10) Product Code/Part # 75CE-B, UDI/DI 00732094209570; 11) Product Code/Part # 75CT-B, UDI/DI 00732094209518; 12) Product Code/Part # 75CT-BR, UDI/DI 00732094322491; 13) Product Code/Part # 75CX-B, UDI/DI 00732094209464; 14) Product Code/Part # 75-HCA-CTB, UDI/DI 00732094240597; 15) Product Code/Part # 75-HCA-MTB, UDI/DI 00732094240603; 16) Product Code/Part # 75ME-B, UDI/DI 00732094209419; 17) Product Code/Part # 75MT-B, UDI/DI 00732094209372; 18) Product Code/Part # 75MT-BR, UDI/DI 00732094 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1563-2025%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.