FDA Medical Device Recalls (openFDA)
Chattanooga Corp.: Triton MP-1 Traction Unit
- Recall number
- Z-1215-03
- Recalling firm
- Chattanooga Corp.
- Product
- Triton MP-1 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
- Recall notification was initiated by telephone on 05/30/2003 to the domestic accounts and via email to the foreign accounts.
- Quantity
- 96
- Distribution
- Nationwide. TX, CO, MD, VA, FL, PA, NJ, NY, IN, OH, MI, MO, AL, NV, IL, CA, NM, AR, LA, NE, WA, NC, A, NH, and OK
- Lot, serial or model codes
- Model/Catalogue Nos.: 7961 (120 Volt) and 7963 (220 Volt); Serial Numbers: 4231 - 4246, 6806 - 6809, 6815, 6818 ¿ 6819, 6824, 6851, 6856 ¿ 6859, 6863, 6870 ¿ 6873, 6878 ¿ 6919, 6921 ¿ 6958
- 510(k) numbers
- ["K801643"]
- PMA numbers
- not on file
- Product code
- INW
- 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