Device recall
Z-0709-2008: Caspar Titanium Aneurysm Clip Appliers, Catalog No/Part #: FT430T, Casper…
FDA device recall · Class II · Aesculap Inc
Key facts
| Recall number (Z-number) | Z-0709-2008 |
|---|---|
| Recall event | 46142 |
| Product | Caspar Titanium Aneurysm Clip Appliers, Catalog No/Part #: FT430T, Casper Applier F/Std Ti-Clipsstr 146 mm, Aesculap, Inc., Center Valley, PA. 18034 |
| Product code | HCI |
| Recalling firm | Aesculap Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2008 |
| 510(k) numbers | K940970 |
| FEI number | 2916714 |
At a glance
- 1–9 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