FDA Device recall Z-0045-2015
Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660
- FDA Device
- Class I
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class I recall of Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660 by Covidien, citing covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0045-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-09-18 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Covidien |
| Distribution | US |
Product
Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660
Reason
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
Identifiers
| code_info | Al lot codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0045-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.