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Terminated

DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC.

FDA Recall Z-0156-2007 · Posted 2006-11-07

Recalling FirmLumiport, LLC
Recall StatusTerminated
Product CodeMOQ
Date Initiated2006-09-28
Date Terminated2012-03-13
Product Quantity2480 units

Reason for Recall

Incorrect charger; batteries may overheat , catch fire or explode while being charged with the charger enclosed with the device.

Firm 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.

Root Cause

Other

Distribution Pattern

World wide Distribution-sales by direct mail or internet-USA and Canada

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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