FDA Medical Device Recalls (openFDA)
Chattanooga Corp Inc: VECTRA TRANSPORTABLE, Model No. 2783, Chattanooga Group, Hixson, TN 37343, Made in the USA
- Recall number
- Z-1222-2008
- Recalling firm
- Chattanooga Corp Inc
- Product
- VECTRA TRANSPORTABLE, Model No. 2783, Chattanooga Group, Hixson, TN 37343, Made in the USA
- Status
- Terminated
- Initiated
- 2007-12-17
- Posted
- 2008-06-25
- Terminated
- 2010-02-19
- Reason
- Device malfunction: causing electric shock and burn.
- Root cause
- Device Design
- Action
- Beginning on 12/17/2007, Chattanooga Corp. sent two recall notification letters, via UPS mail, to its consignees informing them of the situation. The letters stated that the recall was to the user level and requested that the user perform the software upgrade, which will eliminate the possibility of shock and burn.
- Quantity
- 615 units
- Distribution
- Worldwide Distribution - including USA
- Lot, serial or model codes
- Serial numbers 1000 - 1615
- 510(k) numbers
- ["K031077"]
- PMA numbers
- not on file
- Product code
- MPH
- 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