Device recall
Z-0856-2012: R2 Adult R2 Non-Radiolucent Multifunction Electrodes, Catalog/REF No. 3200-1715…
FDA device recall · Class II · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-0856-2012 |
|---|---|
| Recall event | 60701 |
| Product | R2 Adult R2 Non-Radiolucent Multifunction Electrodes, Catalog/REF No. 3200-1715, NON-STERILE, MADE IN USA, CONMED CORPORATION, 525 FRENCH ROAD, UTICA, NY 13507 This device, when connected to a monitor/defibrillator has the ability to monitor the electro-cardio function (ECG) of the patient. The… |
| Product code | MLN |
| Recalling firm | ConMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2012 |
| 510(k) numbers | K964469 |
| 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