Z-1614-2018 Class II Terminated
FDA device recall Z-1614-2018 was initiated by Ii - Vi Incorporated on December 13, 2017 and is designated Class II. Reason for recall: Affected diodes incorporated in the laser sights emitted greater than the 5 mW limit. The recall status is terminated (terminated April 22, 2020). Affected quantity: 323,972.
Recall Details
- Product Type
- Devices
- Report Date
- June 13, 2018
- Initiation Date
- December 13, 2017
- Termination Date
- April 22, 2020
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 323,972
Product Description
11-VI Incorporated Laser diode component Non-certified laser diode component used in laser sights for firearms
Reason for Recall
Affected diodes incorporated in the laser sights emitted greater than the 5 mW limit.
Distribution Pattern
US Distribution to Oregon.
Code Information
Model Numbers: 25-0655 & 25-0657