Device recall
Z-0043-2015: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation…
FDA device recall · Class I · Covidien LLC
Key facts
| Recall number (Z-number) | Z-0043-2015 |
|---|---|
| Recall event | 69257 |
| Product | Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R |
| Product code | DRO |
| Recalling firm | Covidien LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 24, 2017 |
| 510(k) numbers | K012218 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database