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Recall Observatory FDA recall evidence

Device product

Fluoroscan Mini C-arm InSight, software versions 1.x, 2.x, 3.x The device is a Mini C-arm Fluroscopic Imaging System designed to provide physicians with general fluoroscopic visualization of a patient, including but no limited to surgical orthopedic and podiatry use, critical and emergency procedures, and light anatomy imaging situation.

Z-1326-2013

April 25, 2013

Class II

Product summary

Firm
Hologic, Inc.
Event
Event 65028
Status
Terminated
Classification
Class II
Quantity
287
Official record key
device-enforcement:Z-1326-2013

Official wording

Reason: The audible alarm to alert the operator when cumulative irradiation time reaches five minutes is not accurate and the total cumulative irradiation time is not accurate.

Code information: Serial numbers per recall strategy.

Distribution pattern: Worldwide distribution: USA (nationwide) and countries of: DE, RU, AU, IT, GB, ES, FR, KR, ZA, CA, AR, LT, TW, CN, BE, AT, JP, QA, SA, SG, HK, SI, NL, and SE.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The audible alarm to alert the operator when cumulative irradiation time reaches five minutes is not accurate and the total cumulative irradiation time is not accurate.

Field note

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