Device recall
Z-1698-2008: Urethral Warming System-Galil Medical Warming Catheter. The product is contained…
FDA device recall · Class II · Galil Medical
Key facts
| Recall number (Z-number) | Z-1698-2008 |
|---|---|
| Recall event | 47888 |
| Product | Urethral Warming System-Galil Medical Warming Catheter. The product is contained within prostate kits. This product is used in cryosurgery to prevent freezing of tissue. |
| Product code | GEH |
| Recalling firm | Galil Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2008 |
| 510(k) numbers | K012497 |
| FEI number | 3004462490 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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