FDA Device recall Z-1564-2025
Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A 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-1564-2025 |
| 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 Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) ) Product Code/Part # 67MXTX-B; 3) ) Product Code/Part # 67MXXP-B; 4) ) Product Code/Part # 67MXXX-B; 5) ) Product Code/Part # 67NCTP-B; 6) ) Product Code/Part # 67NCTP-B-ECG3A; 7) ) Product Code/Part # 67NCTX-B; 8) ) Product Code/Part # 67NXEX-B; 9) ) Product Code/Part # 67NXTP-B; 10) ) Product Code/Part # 67NXTP-B-ECG3A; 11) ) Product Code/Part # 67NXTX-B; 12) ) Product Code/Part # 67NXXX-B; 13) ) Product Code/Part # 68MCTP-B; 14) ) Product Code/Part # 68MCTP-B-ECG3A; 15) ) Product Code/Part # 68MCTX-B; 16) ) Product Code/Part # 68MCXX-B; 17) ) Product Code/Part # 68MXDX-B; 18) ) Product Code/Part # 68MXEP-B; 19) ) Product Code/Part # 68MXEX-B; 20) ) Product Code/Part # 68MXTP-B; 21) ) Product Code/Part # 68MXTP-B-ECG3A; 22) ) Product Code/Part # 68MXTX-B; 23) ) Product Code/Part # 68MXTX-BR; 24) ) Product Code/Part # 68NCEP-B; 25) ) Product Code/Part # 68NCTP-B; 26) ) Product Code/Part # 68NCTP-B-ECG3A; 27) ) Product Code/Part # 68NCTX-B; 28) ) Product Code/Part # 68NCXP-B; 29) ) Product Code/Part # 68NXEP-B; 30) ) Product Code/Part # 68NXEX-B; 31) ) Product Code/Part # 68NXTP-B; 32) ) Product Code/Part # 68NXTP-B-ECG3A; 33) ) Product Code/Part # 68NXTX-B; 34) ) Product Code/Part # 68NXTX-BR; 35) ) Product Code/Part # 68NXXX-B; 36) ) Product Code/Part # 67MCTP-B; 37) ) Product Code/Part # 67MCTP-B-ECG3A; 38) ) Product Code/Part # 67MCTX-B; 39) ) Product Code/Part # 67MXEX-B; 40) ) Product Code/Part # 67MXTP-B; 41) ) Product Code/Part # 68MXXX-B.
Reason
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Identifiers
| code_info | 1) Product Code/Part # 67MXTP-B-ECG3A, UDI/DI 00732094323788; 2) Product Code/Part # 67MXTX-B, UDI/DI 00732094151244;…1) Product Code/Part # 67MXTP-B-ECG3A, UDI/DI 00732094323788; 2) Product Code/Part # 67MXTX-B, UDI/DI 00732094151244; 3) Product Code/Part # 67MXXP-B, UDI/DI 00732094151237; 4) Product Code/Part # 67MXXX-B, UDI/DI 00732094151220; 5) Product Code/Part # 67NCTP-B, UDI/DI 00732094151190; 6) Product Code/Part # 67NCTP-B-ECG3A, UDI/DI 00732094323771; 7) Product Code/Part # 67NCTX-B, UDI/DI 00732094151183; 8) Product Code/Part # 67NXEX-B, UDI/DI 00732094151145; 9) Product Code/Part # 67NXTP-B, UDI/DI 00732094151138; 10) Product Code/Part # 67NXTP-B-ECG3A, UDI/DI 00732094323764; 11) Product Code/Part # 67NXTX-B, UDI/DI 00732094151121; 12) Product Code/Part # 67NXXX-B, UDI/DI 00732094151107; 13) Product Code/Part # 68MCTP-B, UDI/DI 00732094151060; 14) Product Code/Part # 68MCTP-B-ECG3A, UDI/DI 00732094345919; 15) Product Code/Part # 68MCTX-B, UDI/DI 00732094151053; 16) Product Code/Part # 68MCXX-B, UDI/DI 00732094151039; 17) Product Code/Part # 68MXDX-B, UDI/DI 00732094249187; |
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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-1564-2025%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.