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Recall Observatory FDA recall evidence

Device product

07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-2000-2014

May 28, 2014

Class II

Product summary

Firm
Vascular Technology, Inc.
Event
Event 68512
Status
Terminated
Classification
Class II
Quantity
34
Official record key
device-enforcement:Z-2000-2014

Official wording

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

Code information: LOT NUMBER 1516-37698

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.