Device recall
Z-1174-2010: UROLOGIX CTC Advance" Standard Microwave Catheter (3.0-5.0 cm), CTC Advance"…
FDA device recall · Class II · Urologix, Inc.
Key facts
| Recall number (Z-number) | Z-1174-2010 |
|---|---|
| Recall event | 54703 |
| Product | UROLOGIX CTC Advance" Standard Microwave Catheter (3.0-5.0 cm), CTC Advance" Long Microwave Catheter (4.5+ cm), CTC Advance" Short Microwave Catheter (2.5 -3.5 cm), RTU Plus Balloon, and RTU Plus Handle, Sterile EO, Manufactured by UROLOGIX, INC, 14405 Twenty-First Avenue North, Minneapolis, MN… |
| Product code | MEQ |
| Recalling firm | Urologix, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2012 |
| PMA numbers | P970008 |
| FEI number | 3000718675 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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