Wescam Inc 649 North Service Road West Burlington Canada Ontario 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Wescam Inc 649 North Service Road West Burlington Canada Ontario
Lot Codes / Batch Numbers
Only model numbers.
Products Sold
Only model numbers.
Wescam Inc 649 North Service Road West Burlington Canada Ontario is recalling MX Series Products, Model numbers MX 20, MX 20 High Definition (HD), MX 15, MX 15i (integrated) and due to Products do not comply with 21 CFR 1040.11.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Products do not comply with 21 CFR 1040.11.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026