Device recall
Z-1184-03: 1680 Invisatrace series ECG Electrodes, radiotranslucent clear tape ECG…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-1184-03 |
|---|---|
| Recall event | 26988 |
| Product | 1680 Invisatrace series ECG Electrodes, radiotranslucent clear tape ECG electrode with wet gel. This is a single use, disposable device. Electrodes are packaged and sold as: Cat No 1680-001 (1 unit per pouch/30 per box); Cat No 1680-003 (3 units per pouch/30 per box); Cat No 1680-005 (5 units per… |
| Product code | DRX |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2005 |
| 510(k) numbers | K991105 |
| FEI number | 3001451571 |
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