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Terminated

MX Series Products, Model numbers MX 20, MX 20 High Definition (HD), MX 15, MX 15i (integrated) and MX 15 HDi. Long range surveillance, target designation.

FDA Recall Z-0172-2010 · Posted 2009-12-16

Recalling FirmWescam Inc
Recall StatusTerminated
Product CodeRET
Date Initiated2009-08-01
Date Terminated2013-01-15
Product Quantity306 total

Reason for Recall

Products do not comply with 21 CFR 1040.11.

Firm Action

L-3 Wescam has issued notification of the MX Series Products describing a non-compliance with 1040.11(b). The notice instructs customers to refrain from using the infrared laser illuminator, based on a serious eye hazard from viewing the direct or reflected laser emission. Products will be repaired or removed if they cannot be repaired and a refund will be implemented.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

Nationwide Distribution

Official Source

View FDA Recall →

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

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