FDA Medical Device Recalls (openFDA)
Chattanooga Corp.: Triton T-700 Traction Unit
- Recall number
- Z-1210-03
- Recalling firm
- Chattanooga Corp.
- Product
- Triton T-700 Traction Unit,
- Status
- Terminated
- Initiated
- 2003-05-30
- Posted
- 2003-09-11
- Terminated
- 2004-05-07
- Reason
- Product contains an improper bracket for the transducer.
- Root cause
- Other
- Action
- Notification of the manufacturing defect and recall was initiated by telephone on 05/30/2003 to the domestic accounts and via email to the foreign accounts.
- Quantity
- 18 units
- Distribution
- IL, CA, TX, OH, FL, LA, WA, NC and DC
- Lot, serial or model codes
- Model/Catalogue Nos.: 7950 (120 Volt) and 7952 (220 Volt); Serial Numbers: 6211-6230, 1907 & 1920
- 510(k) numbers
- ["K801643"]
- PMA numbers
- not on file
- Product code
- ITF
- Firm FEI
- 1000342033
- Firm city
- Hixson
- Firm state
- TN
- 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