Device recall
Z-1185-03: 1690 Ultratrace Series ECG Electrodes, clear tape ECG electrode with wet gel…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-1185-03 |
|---|---|
| Recall event | 26988 |
| Product | 1690 Ultratrace Series ECG Electrodes, clear tape ECG electrode with wet gel. This is a single use, disposable device. Electrodes are packaged and sold as: Cat No 1690-001 (1 unit per pouch/30 per box); 1690-003 (3 units per pouch/30 per box); 1690-005 (5 units per pouch/50 per box); 1690-010 (50… |
| Product code | DRX |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2005 |
| 510(k) numbers | K905446 |
| 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