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Recall Observatory FDA recall evidence

Device product

VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS 63CM/45DEG/D0 SHEATH VXS2112 VERSACROSS SHEATH (63CM 45DEG D0)-J Used for the percutaneous introduction of various types of cardiovascular catheters and guidewires to all heart chambers, including the left atrium via transseptal perforation / puncture.

Z-2105-2025

June 10, 2025

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 97036
Status
Ongoing
Classification
Class II
Quantity
14,724
Official record key
device-enforcement:Z-2105-2025

Official wording

Reason: 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.

Code information: VXS0201 UDI-DI 00685447020301 Lot 35800622; VXS2112 UDI-DI 00685447019251 Lot 35892045

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, Hong Kong, and Japan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.