PlainRecalls
FDA Devices Critical Class I Terminated

MediChoice¿ Multifunction Electrode Part Number: MC171 OH

Reported: October 22, 2014 Initiated: September 18, 2014 #Z-0047-2015

Product Description

MediChoice¿ Multifunction Electrode Part Number: MC171 OH

Reason for Recall

Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

Details

Recalling Firm
Covidien LLC
Units Affected
330 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?
MediChoice¿ Multifunction Electrode Part Number: MC171 OH. Recalled by Covidien LLC. Units affected: 330 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
Which agency issued this recall?
This recall was issued by the FDA Devices on October 22, 2014. Severity: Critical. Recall number: Z-0047-2015.