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FDA (Device enforcement)Recalled 2025-06-10class ii

Boston Scientific Corporation: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM 55DEG Used for the percutaneous introduction of vari

Hazard

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.

Details from the source

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: TF85-32-63-45 UDI-DI 00685447005391 Lots 35508747 35644132 35746496 35913449; TF85-32-63-55 UDI-DI 00685447005407 Lots 35508748 35738145

UPC codes

00685447005391, 00685447005407

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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