FDA Recall
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.
Recall: Z-2316-2018
·
Initiated May 8, 2018
Recall
- Recall Number
- Z-2316-2018
- Event Number
- 80392
- Firm
- Wescam Inc
- FEI Number
- 3000173214
- Product Code
- REP
- Status
- Terminated
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- May 8, 2018
- Terminated
- August 24, 2021
- Address
- 649 North Service Rd, Burlington Canada Ontario
Description
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
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.
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].
Distribution
US Nationwide Distribution
Quantity
29