Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location.
Reason for recall: Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis in worst case scenario. Potential punctures may go undetected in clinical settings due to small size and variable location. Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Hong Kong, and Japan. Quantity: 14,724 Lot/code info: VXS0201 UDI-DI 00685447020301 Lot 35800622; VXS2112 UDI-DI 00685447019251 Lot 35892045
00685447020301, 00685447019251
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.