Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A
FDA device recall Z-0418-05 · posted 2005-01-25 · Terminated
Recall details
- Recalling firm
- Weck
- Reason for recall
- Some stylets were not bent sufficiently during the packaging process to preclude them from sliding back into the cannula during shipment.
- Action taken
- Consignees were notified by letter sent via Federal Express on/about 05/21/2003.
- Root cause
- Other
- Status
- Terminated
- Product code
- GDO
- Quantity affected
- 667 units
- Distribution
- Nationwide
- Date initiated
- 2003-05-21
- Date posted
- 2005-01-25
- Date terminated
- 2005-01-31
- Location
- Research Triangle Park, NC
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