Device recall
Z-2383-2010: 3M Red Dot Monitoring Electrode, Catalog #2560 & Novaplus Universal Monitoring…
FDA device recall · Class II · 3M Company / Medical Division
Key facts
| Recall number (Z-number) | Z-2383-2010 |
|---|---|
| Recall event | 56488 |
| Product | 3M Red Dot Monitoring Electrode, Catalog #2560 & Novaplus Universal Monitoring Electrode #V2560, used for ECG monitoring. |
| Product code | DRX |
| Recalling firm | 3M Company / Medical Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| 510(k) numbers | K970796 |
| FEI number | 2110898 |
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