FDA Medical Device Recalls (openFDA)
Daavlin Distributing Company: 3 Series Full Body Phototherapy Device with Smart Touch Control System, Model All Touch Control System, Model #ASNBSM-2424 units manufactured between 6/5/03 and 4/30/04..
- Recall number
- Z-1234-04
- Recalling firm
- Daavlin Distributing Company
- Product
- 3 Series Full Body Phototherapy Device with Smart Touch Control System, Model All Touch Control System, Model #ASNBSM-2424 units manufactured between 6/5/03 and 4/30/04..
- Status
- Terminated
- Initiated
- 2003-09-01
- Posted
- 2004-07-30
- Terminated
- 2007-07-24
- Reason
- Software errors cause the unit to not deliver the prescribed therapy and do not allow the patient records to be saved.
- Root cause
- Other
- Action
- The firm has software patches to correct the programming problems as they are reported by the users. These patches are being installed either by a service representative for the manufacturer or by the customer
- Quantity
- 12 units distributed domestically and 5 units distributed to foreign accounts.
- Distribution
- Nation wide plus Canada, the Philippines, Saudi Arabia, Turkey & Germany
- Lot, serial or model codes
- All Touch Control System, Model All Touch Control System, Model #ASNBSM-2424 units manufactured between 6/5/03 and 4/30/04.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FTC
- Firm FEI
- 1526255
- Firm city
- Bryan
- Firm state
- OH
- 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