Device recall
Z-1317-2013: PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No…
FDA device recall · Class II · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-1317-2013 |
|---|---|
| Recall event | 65112 |
| Product | PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C. The PadPro(R) Adult Radiotransparent Multifunction Electrodes with Carbon Leadwires and Medtronic(R) Connector are intended to be used in external pacing, defibrillation and monitoring applications |
| Product code | MKJ |
| Recalling firm | ConMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2015 |
| 510(k) numbers | K014209 |
| FEI number | 3001451571 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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