# FDA recall Z-1566-2025

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

## Product

Welch Allyn Green Series 777 Wall System, Product Code/Part Numbers:    1) 77791-2MP2X;   2) 77791-2MP2XL;   3) 77791-2MPX;   4) 77791-2MPX-HS;   5) 77791-2MPXL;   6) 77796-2MPX;   7) 77796-2MPXL.

## 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-1566-2025
- **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-1566-2025

## Citation

> AI Analytics. FDA recall Z-1566-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1566-2025. Source: US FDA. Licensed CC0.

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