Device recall
Z-1452-06: 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. CryoCath Technologies…
FDA device recall · Class III · CryoCath Technologies Inc.
Key facts
| Recall number (Z-number) | Z-1452-06 |
|---|---|
| Recall event | 36087 |
| Product | 7F Freezor Cardiac Cryoablation catheter, REF # 207F1. CryoCath Technologies Inc. |
| Product code | LPB |
| Recalling firm | CryoCath Technologies Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 16, 2007 |
| PMA numbers | P020045 |
| FEI number | 3002648230 |
At a glance
- None 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