Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

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

FDA Recall Z-2316-2018 · Posted None

Recalling FirmWescam Inc
Recall StatusTerminated
Product CodeREP
Date Initiated2018-05-08
Date Terminated2021-08-24
Product Quantity29

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.

Firm 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 [email protected].

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑