FDA Medical Device Recalls (openFDA)
Lumiport, LLC: DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC.
- Recall number
- Z-0156-2007
- Recalling firm
- Lumiport, LLC
- Product
- DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC.
- Status
- Terminated
- Initiated
- 2006-09-28
- Posted
- 2006-11-07
- Terminated
- 2012-03-13
- Reason
- Incorrect charger; batteries may overheat , catch fire or explode while being charged with the charger enclosed with the device.
- Root cause
- Other
- Action
- Individual customers were contacted through e-mail and/or telephone beginning 09/28/2006. They were told to stop charging and using their current DermaStyle and to destroy it to prevent accidental usage. New replacements will be mailed to all customers.
- Quantity
- 2480 units
- Distribution
- World wide Distribution-sales by direct mail or internet-USA and Canada
- Lot, serial or model codes
- All units sold before 08/01/2006.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MOQ
- Firm FEI
- 3005952043
- Firm city
- Provo
- Firm state
- UT
- 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