Wescam Inc: Medical Device Recall in 2018 - (Recall #: Z-2316-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 8, 2018

Date Posted: July 25, 2018

Recall Number: Z-2316-2018

Event ID: 80392

Reason for Recall:

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.

Status: Terminated

Product Quantity: 29

Code Information:

L3 Wescam MX-10, part numbers 44620-203, 44620-211, 44620-213, 44620-215, 44620-221,4620-258, 44620-263, 44620-277, 45840-13, 45840-20, and 45840-23

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated