Covidien LLC: Medical Device Recall in 2014 - (Recall #: Z-0047-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

MediChoice¿ Multifunction Electrode Part Number: MC171 OH

Product Classification:

Class I

Date Initiated: September 18, 2014

Date Posted: October 22, 2014

Recall Number: Z-0047-2015

Event ID: 69257

Reason for Recall:

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

Status: Terminated

Product Quantity: 330 pairs

Code Information:

Al lot codes

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated