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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69257

6 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 18, 2014
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Covidien LLC

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 6

Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R

Z-0043-2015
Recall number
Z-0043-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
317,550 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs Defibrillators

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

All lots

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.

device · product 2 of 6

Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Number: 22660PC

Z-0044-2015
Recall number
Z-0044-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
9,850 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

device · product 3 of 6

Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660

Z-0045-2015
Recall number
Z-0045-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
31,590 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

device · product 4 of 6

Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006

Z-0046-2015
Recall number
Z-0046-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
133,930 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

device · product 5 of 6

MediChoice¿ Multifunction Electrode Part Number: MC171 OH

Z-0047-2015
Recall number
Z-0047-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
330 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.

device · product 6 of 6

Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A

Z-0048-2015
Recall number
Z-0048-2015
Initiated
September 18, 2014
Classification
Class I
Status
Terminated
Recalling firm
Covidien LLC
Quantity
151,210 pairs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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.