Device recall
Z-0728-03: SurgiFrost Cryosurgical Probes
FDA device recall · Class II · Endocare Inc
Key facts
| Recall number (Z-number) | Z-0728-03 |
|---|---|
| Recall event | 25856 |
| Product | SurgiFrost Cryosurgical Probes |
| Product code | GEH |
| Recalling firm | Endocare Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2003 |
| FEI number | 3008262715 |
At a glance
- None 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