FDA recall Z-0822-2018

Accord Media, LLC · Class II · device

Product

Truth Renew Plus

Reason for recall

Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Distribution

US Nationwide

Key facts

Status
Terminated
Initiation date
2017-12-04
Report date
2018-03-07
Termination date
2020-05-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
New York, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0822-2018