FDA Device recall Z-2316-2018
MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions fro…
- FDA Device
- Class II
- terminated
- Published 2018-07-25
On 2018-07-25 the FDA classified a Class II recall of MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions fro… by Wescam, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2316-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-08 |
| Published | 2018-07-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Wescam |
| Distribution | US |
Product
MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.
Reason
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.
Identifiers
| code_info | 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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2316-2018%22
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