Wescam Inc recalls MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surve…

Recall date

May 8, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2316-2018

FDA classification

Class II

Brand / firm

Wescam Inc

Sold / distributed

US Nationwide Distribution

Why it was recalled

Product has a nominal ocular hazard distance (NOHD) that is longer than specified and persons could be exposed to light in excess of the exposure limit.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.