FDA Device recall Z-1562-2025
Welch Allyn Connex Integrated Wall System, Product Code/Part Numbers: 1) 84MTVE2-4
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn Connex Integrated Wall System, Product Code/Part Numbers: 1) 84MTVE2-4 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-1562-2025 |
| 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 Connex Integrated Wall System, Product Code/Part Numbers: 1) 84MTVE2-4; 2) 84MTVE2-6; 3) 84MTVE2-B; 4) 84MTVE2-US; 5) 84MTVEC-6; 6) 84MTVEC-B; 7) 84MTVEP-B; 8) 84MTVEX-4; 9) 84MTVX2-4; 10) 84MTVX2-6; 11) 84MTVX2-B; 12) 84MTVX2-US; 13) 84MTVXC-4; 14) 84MTVXC-B; 15) 84MTVXP-2; 16) 84MTVXP-4; 17) 84MTVXP-B; 18) 84MTVXX-2; 19) 84MXVEC-4; 20) 84MXVEC-B; 21) 84MXVEP-4; 22) 84MXVEP-B; 23) 84NTVE2-6; 24) 84NTVE2-B; 25) 84NTVE2-US; 26) 84NTVEC-B; 27) 84NTVX2-6; 28) 84NTVX2-B; 29) 84NTVX2-US; 30) 84NTVXC-4; 31) 84NTVXC-B; 32) 84NTVXP-B; 33) 84NXVEC-4; 34) 84NXVEC-6; 35) 84NXVEC-B; 36) 84XTVXC-2; 37) 84XTVXC-B; 38) 85MTVE3-2; 39) 85MTVE3-4; 40) 85MTVE3-B; 41) 85MTVE3-US; 42) 85MTVEC-4; 43) 85MTVEC-B; 44) 85MTVEP-2; 45) 85MTVEP-B; 46) 85MTVX3-4; 47) 85MTVX3-B; 48) 85MTVX3-US; 49) 85MTVXC-6; 50) 85MTVXC-B; 51) 85MTVXX-6; 52) 85MXVEC-2; 53) 85MXVEC-4; 54) 85MXVEC-B; 55) 85MXVEP-4; 56) 85NTVE3-4; 57) 85NTVE3-6; 58) 85NTVE3-B; 59) 85NTVE3-US; 60) 85NTVEC-B; 61) 85NTVEP-2; 62) 85NTVEP-6; 63) 85NTVEP-B; 64) 85NTVX3-6; 65) 85NTVX3-B; 66) 85NTVX3-US; 67) 85NTVXC-B; 68) 85NTVXP-2; 69) 85NTVXP-B; 70) 85NXVEC-4; 71) 85NXVEC-B; 72) 85NXVEP-6.
Reason
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Identifiers
| code_info | 1) Product Code/Part # 84MTVE2-4, UDI/DI 00732094350548; 2) Product Code/Part # 84MTVE2-6, UDI/DI 00732094350463; 3)…1) Product Code/Part # 84MTVE2-4, UDI/DI 00732094350548; 2) Product Code/Part # 84MTVE2-6, UDI/DI 00732094350463; 3) Product Code/Part # 84MTVE2-B, UDI/DI 00732094349856; 4) Product Code/Part # 84MTVE2-US, UDI/DI 00732094350388; 5) Product Code/Part # 84MTVEC-6, UDI/DI 00732094058741; 6) Product Code/Part # 84MTVEC-B, UDI/DI 00732094058734; 7) Product Code/Part # 84MTVEP-B, UDI/DI 00732094119442; 8) Product Code/Part # 84MTVEX-4, UDI/DI 00732094198638; 9) Product Code/Part # 84MTVX2-4, UDI/DI 00732094350531; 10) Product Code/Part # 84MTVX2-6, UDI/DI 00732094350456; 11) Product Code/Part # 84MTVX2-B, UDI/DI 00732094349849; 12) Product Code/Part # 84MTVX2-US, UDI/DI 00732094350371; 13) Product Code/Part # 84MTVXC-4, UDI/DI 00732094058550; 14) Product Code/Part # 84MTVXC-B, UDI/DI 00732094058512; 15) Product Code/Part # 84MTVXP-2, UDI/DI 00732094198607; 16) Product Code/Part # 84MTVXP-4, UDI/DI 00732094058390; 17) Product Code/Part # 84MTVXP-B, UDI/DI 00732094058352; 18) |
|---|
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-1562-2025%22
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