Caspar Titanium Aneurysm Clip Appliers, Catalog No/Part #: FT430T, Casper Applier F/Std Ti-Clipsstr 146 mm, Aesculap, In
FDA device recall Z-0709-2008 · posted 2008-01-29 · Terminated
Recall details
- Recalling firm
- Aesculap Inc
- Reason for recall
- Breakage: the inner rod of the applier may corrode and break
- Action taken
- The recalling firm issued an Import Recall Notice, on or about December 18, 2007, to all their customers to inform them of the problem and the need to return the devices .
- Root cause
- Device Design
- Status
- Terminated
- Product code
- HCI
- Quantity affected
- 84 clips
- Distribution
- Worldwide- USA hospitals in AZ, CA, CO, IL, KY, MI, MS, ND, NM, NY, OH, OK, PA, TX, VA, WA, and WI, to sales representatives in NC, OK, and MO and shipped to distributors in CA and Canada.
- Date initiated
- 2007-11-01
- Date posted
- 2008-01-29
- Date terminated
- 2008-03-28
- Location
- Center Valley, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| YASARGIL, CASPAR, VARIO CLIP APPLIERS (K940970) | Aesculap, Inc. | 1995-01-24 |