# FDA recall Z-1562-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-03-21.

## 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-

## Reason for recall

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1562-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-21
- **Report date:** 2025-04-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1562-2025

## Citation

> AI Analytics. FDA recall Z-1562-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1562-2025. Source: US FDA. Licensed CC0.

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