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Recall Observatory FDA recall evidence

Device product

VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-2001-2014

May 28, 2014

Class II

Product summary

Firm
Vascular Technology, Inc.
Event
Event 68512
Status
Terminated
Classification
Class II
Quantity
25
Official record key
device-enforcement:Z-2001-2014

Official wording

Reason: Report of the product penetrating the sterile barrier; this could render the product unsterile.

Code information: LOT NUMBER 11786-37683

Distribution pattern: Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Report of the product penetrating the sterile barrier; this could render the product unsterile.