Recall Z-1566-2025— Baxter Healthcare Corporation

Name: FDA recall Z-1566-2025
Creator: U.S. Food and Drug Administration
Published: 2025-03-21

Class II · Ongoing

Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2025-03-21. FDA's recall record names no specific 510(k) clearance for this event. 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: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs..

Recalling firm: Baxter Healthcare Corporation
Classification: Class II
Status: Ongoing
Initiated: 2025-03-21
Firm location: Deerfield, IL, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.