Company:Lockheed-Martin Aculight
Date of Enforcement Report 7/6/2011
Class ll:
PRODUCT
Lockheed Martin Aculight Capella-r 1850 Laser. The Capella Laser is intended for use in user-defined scientific applications and non-human-use research on infrared nerve stimulation. Recall # Z-2069-2011
REASON
It has been determined that there are certain software driven operating sequences involving off-on cycling of the key-switch that do not result in a reset of the Stim Enable button, and emissions can resume after a standard 5 second countdown without pressing this button a second time.
RECALLING FIRM/MANUFACTURER
Lockheed-Martin Aculight, Bothell, WA, by letter on November 19, 2010. Firm initiated recall is ongoing.
VOLUME OF PRODUCT IN COMMERCE
17 units
DISTRIBUTION
Nationwide
