# FDA recall Z-1568-2025

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

## Product

Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits labeled as:    1. WELCH ALLYN 2-Piece Reusable Blood Pressure Cuff Kits, Product Code/Part Numbers:    2. WELCH ALLYN Reusable Blood Pressure Cuff Kit, Product Code/Part Numbers:  410519, 5090-41, 5098-20.

## 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-1568-2025
- **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-1568-2025

## Citation

> AI Analytics. FDA recall Z-1568-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1568-2025. Source: US FDA. Licensed CC0.

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