FDA Medical Device Recalls (openFDA)
Conmed Electrosurgery: Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS, Conmed Corporation
- Recall number
- Z-1507-06
- Recalling firm
- Conmed Electrosurgery
- Product
- Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS, Conmed Corporation
- Status
- Terminated
- Initiated
- 2006-09-05
- Posted
- 2006-09-19
- Terminated
- 2006-10-26
- Reason
- Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.
- Root cause
- Other
- Action
- Domestic customers were notified by letter on 09/01/2006 and international accounts were notified by letter on 09/07/2006.
- Quantity
- 19 units (International)
- Distribution
- Worldwide, including USA, Australia, Canada, France, Japan, Korea, New Zealand, Saudi Arabia, UK.
- Lot, serial or model codes
- Serial numbers: 06GGN 001 thru 009, 06FGN 001 thru 010.
- 510(k) numbers
- ["K020135"]
- PMA numbers
- not on file
- Product code
- GEI
- Firm FEI
- 3004491689
- Firm city
- Centennial
- Firm state
- CO
- 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