# FDA recall Z-1563-2025

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

## 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 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-1563-2025
- **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-1563-2025

## Citation

> AI Analytics. FDA recall Z-1563-2025. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1563-2025. Source: US FDA. Licensed CC0.

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