# FDA recall Z-2316-2018

> **Wescam Inc** · Class II · device recall initiated 2018-05-08.

## 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 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.

## Distribution

US Nationwide  Distribution

## Key facts

- **Recall number:** Z-2316-2018
- **Recalling firm:** Wescam Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-08
- **Report date:** 2018-07-25
- **Termination date:** 2021-08-24

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Burlington, Ontario, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2316-2018

## Citation

> AI Analytics. FDA recall Z-2316-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2316-2018. Source: US FDA. Licensed CC0.

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