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FDA Medical Device Recalls (openFDA)

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

Recall number
Z-2316-2018
Recalling firm
Wescam Inc
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.
Status
Terminated
Initiated
2018-05-08
Posted
not on file
Terminated
2021-08-24
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.
Root cause
Radiation Control for Health and Safety Act
Action
Firm sent a Service Bulletin dated June 2018 to customers. The Bulletin identified the affected product, problem and actions to be taken. For question call 888-5-WESCAM or email support.wescam@L3T.com.
Quantity
29
Distribution
US Nationwide Distribution
Lot, serial or model codes
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
510(k) numbers
not on file
PMA numbers
not on file
Product code
REP
Firm FEI
3000173214
Firm city
Burlington Canada
Firm state
Ontario
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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