Device recall
Z-0757-2007: PADPRO ADULT Radiotranslucent Pad w/Medtronic connector, REF/Catalog #2516M. RX…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-0757-2007 |
|---|---|
| Recall event | 37495 |
| Product | PADPRO ADULT Radiotranslucent Pad w/Medtronic connector, REF/Catalog #2516M. RX ONLY. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes. Made in USA for: CONMED CORPORATION Utica, New York, 13502. |
| Product code | MLN |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 16, 2012 |
| 510(k) numbers | K020203 |
| FEI number | 3001451571 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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