Recall Z-1361-2018— Crimson Trace Corporation
Class II · Terminated
Class II FDA medical device recall by Crimson Trace Corporation, initiated 2017-10-10, terminated 2019-11-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for personal defense and target acquisition.. Reason: A previously "in specification" Finished Product with a Model 25-0657 diode had power output higher than 5 mW..
- Recalling firm
- Crimson Trace Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-10-10
- Terminated
- 2019-11-22
- Firm location
- Wilsonville, OR, United States
Product description
Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for personal defense and target acquisition.
Reason for recall
A previously "in specification" Finished Product with a Model 25-0657 diode had power output higher than 5 mW.
Data sourced from openFDA. This site is unofficial and independent of the FDA.