FDA Medical Device Recalls (openFDA)
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.
- Recall number
- Z-0418-05
- Recalling firm
- Weck
- Product
- 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.
- Status
- Terminated
- Initiated
- 2003-05-21
- Posted
- 2005-01-25
- Terminated
- 2005-01-31
- 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
- Lot, serial or model codes
- Catalogue #809600, Lot #978933 & 978934
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GDO
- Firm FEI
- 3005747797
- Firm city
- Research Triangle Park
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28