Device recall
Z-0602-03: Bard Orbiter ST Artrial Mapping Steerable Catheter Item Numbers 320001 7FAM00001…
FDA device recall · Class II · C. R.Bard, Inc./Electrophysiology Division
Key facts
| Recall number (Z-number) | Z-0602-03 |
|---|---|
| Recall event | 25401 |
| Product | Bard Orbiter ST Artrial Mapping Steerable Catheter Item Numbers 320001 7FAM00001 7FAM00010 7FAM00019 7FAM0008B 7FAM0017B 320002 7FAM00002 7FAM00011 7FAM00020 7FAM0009B 7FAM0018B 320003 7FAM00003 7FAM00012 7FAM0001B 7FAM0010B 7FAM0019B 320004 7FAM00004 7FAM00013 7FAM0002B 7FAM0011B 7FAM0020B 320005… |
| 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