Covidien Medi-Trace Cadence and Kendall Adult Multi-Function… — Class I medical device recall Z-0043-2015
Terminated recall by Covidien LLC, reported 2014-10-22, distributed nationwide. Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR
| Recall number | Z-0043-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, Mansfield, MA, United States |
| Recall initiated | 2014-09-18 |
| Classified | 2014-10-16 |
| Reported by FDA | 2014-10-22 |
| Terminated | 2017-05-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, BR, CA, CH, CL, DE, ES, FI, FR, GB, GR, IE, IL, IT, NO, NZ, PH, PL, PT, SE, TW |
| Quantity | 317,550 pairs |
| Model numbers | 22660R |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0043-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.