RecallRadar

FDA Device recall Z-1566-2025

Welch Allyn Green Series 777 Wall System, Product Code/Part Numbers: 1) 77791-2MP2X

On 2025-04-23 the FDA classified a Class II recall of Welch Allyn Green Series 777 Wall System, Product Code/Part Numbers: 1) 77791-2MP2X by Baxter Healthcare, citing undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1566-2025
ClassificationClass II
Statusongoing
Initiated2025-03-21
Published2025-04-23
Last updated2026-09-13 11:57 UTC
CompanyBaxter Healthcare
Distributionn/a

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.

Identifiers

code_info
1) Product Code/Part # 77791-2MP2X, UDI/DI 00732094066890; 2) Product Code/Part # 77791-2MP2XL, UDI/DI 00732094201833;…1) Product Code/Part # 77791-2MP2X, UDI/DI 00732094066890; 2) Product Code/Part # 77791-2MP2XL, UDI/DI 00732094201833; 3) Product Code/Part # 77791-2MPX, UDI/DI 00732094066876; 4) Product Code/Part # 77791-2MPX-HS, UDI/DI 00732094231045; 5) Product Code/Part # 77791-2MPXL, UDI/DI 00732094201826; 6) Product Code/Part # 77796-2MPX, UDI/DI 00732094066289; 7) Product Code/Part # 77796-2MPXL, UDI/DI 00732094184013; Lot Number 24-314 & lower

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1566-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.