Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R
Reported: October 22, 2014 Initiated: September 18, 2014 #Z-0043-2015
Product Description
Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R
Reason for Recall
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs Defibrillators
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- 317,550 pairs
- Distribution
- Worldwide Distribtion-USA (nationwide) including Puerto Rico and the countries of Canada Greece Israel Belgium Finland France Germany Great Britain Ireland Italy Norway Poland Portugal Spain Sweden Switzerland Brazil Chile Philippines Taiwan Australia New Zealand.
- Location
- Mansfield, MA
Frequently Asked Questions
What product was recalled? ▼
Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R. Recalled by Covidien LLC. Units affected: 317,550 pairs.
Why was this product recalled? ▼
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs Defibrillators
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2014. Severity: Critical. Recall number: Z-0043-2015.
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