# FDA recall Z-1564-2025

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

## 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

## 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-1564-2025
- **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-1564-2025

## Citation

> AI Analytics. FDA recall Z-1564-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1564-2025. Source: US FDA. Licensed CC0.

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