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Recall Observatory FDA recall evidence

Device product

ICEfx Cryoablation System, portable helium-free desktop cryoablation unit, Material Numbers (UPN) FPRCH8000, FPRCH8000-02, H749396118000

Z-2550-2025

August 18, 2025

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 97466
Status
Ongoing
Classification
Class II
Quantity
18 units
Official record key
device-enforcement:Z-2550-2025

Official wording

Reason: Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.

Code information: FPRCH8000 UDI-DI: 00859019006370, Serial Numbers: ICP0305, ICP0369, ICP0338; FPRCH8000-02 UDI-DI: 00859019006417, Serial Numbers: 86643865, 108415728, 88589050, 108470986, 89392275, 108612524, 107799735, ICP0299, 107887794, 3779, 108254011, IF0096 108312221, 104733618; H749396118000 UDI-DI: 00191506014995, Serial Numbers: 106066356, 107851990

Distribution pattern: Worldwide - US Nationwide and the countries of Canada, France, Germany and Italy. (Preventive Maintenance Kit distributed to Canada only.)

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.