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Recall Observatory FDA recall evidence

Device product

Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

Z-1184-2013

April 08, 2013

Class II

Product summary

Firm
Covidien LLC
Event
Event 64868
Status
Terminated
Classification
Class II
Quantity
133470 (sets of 2)
Official record key
device-enforcement:Z-1184-2013

Official wording

Reason: Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient

Code information: Lot Numbers: 226543X, 230054X , 230814X, 232182X, 232805X, 234245X, 304667X, 301844X, 300446X, 305320X

Distribution pattern: Worldwide Distribution-USA (nationwide) and the countries of Korea, Japan, Canada, Australia, Brazil, Belgium, Singapore, and South Africa.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Defibrillation Electrodes may arc/spark result in thermal damage to the leadwire, which could render the device incapable of delivering the appropriate energy or shock to the patient

Field note

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