FDA Medical Device Recalls (openFDA)
TissueLink Medical, Inc.: ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device
- Recall number
- Z-1416-04
- Recalling firm
- TissueLink Medical, Inc.
- Product
- ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device
- Status
- Terminated
- Initiated
- 2004-07-22
- Posted
- 2004-09-01
- Terminated
- 2004-10-04
- Reason
- Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing.
- Root cause
- Other
- Action
- TissueLink notified the sales force on 7/22/04 to visit each account and retreive product at the hospital level.
- Quantity
- 96 units
- Distribution
- Nationwide
- Lot, serial or model codes
- Lot Numbers: TLK17300, TLB02400
- 510(k) numbers
- ["K020574","K022532"]
- PMA numbers
- not on file
- Product code
- GEI
- Firm FEI
- 1000517638
- Firm city
- Dover
- Firm state
- NH
- 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