Device recall
Z-0603-03: Bard Orbiter PV Steerable Catheter Item #: 320100 (Marketed in Europe Only)
FDA device recall · Class II · C. R.Bard, Inc./Electrophysiology Division
Key facts
| Recall number (Z-number) | Z-0603-03 |
|---|---|
| Recall event | 25401 |
| Product | Bard Orbiter PV Steerable Catheter Item #: 320100 (Marketed in Europe Only) |
| Recalling firm | C. R.Bard, Inc./Electrophysiology Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2012 |
| FEI number | 1000120754 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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