Device recall
Z-1111-04: Metricath Balloon Catheter model #RX183670
FDA device recall · Class II · Angiometrx Inc.
Key facts
| Recall number (Z-number) | Z-1111-04 |
|---|---|
| Recall event | 29481 |
| Product | Metricath Balloon Catheter model #RX183670 |
| Product code | DQO |
| Recalling firm | Angiometrx Inc. |
| Recall class | Class II |
| Status | Terminated on November 17, 2005 |
| 510(k) numbers | K024000 |
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