Recall Z-0418-05 ยท GDO Applier, Surgical, Clip
Weck
Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA.
| Date | Jan 25, 2005 (initiated May 21, 2003) |
| Status | Terminated |
| Reason | Some stylets were not bent sufficiently during the packaging process to preclude them from sliding back into the cannula during shipment. |
| Root cause | Other |
| Action | Consignees were notified by letter sent via Federal Express on/about 05/21/2003. |
| Quantity | 667 units |
| Distribution | Nationwide |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.