Device recall
Z-2545-2015: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-2545-2015 |
|---|---|
| Recall event | 71963 |
| Product | MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC |
| Product code | DRO |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2017 |
| 510(k) numbers | K012218 |
| FEI number | 1219930 |
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