Recall Z-0001-2022— Potomac River Group, Corp.
Class II · Ongoing
Class II FDA medical device recall by Potomac River Group, Corp., initiated 2021-04-21. FDA's recall record names no specific 510(k) clearance for this event. Product: RAPTAR Laser Range Finders. Reason: RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator..
- Recalling firm
- Potomac River Group, Corp.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-04-21
- Firm location
- Ashburn, VA, United States
Product description
RAPTAR Laser Range Finders
Reason for recall
RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator.
Data sourced from openFDA. This site is unofficial and independent of the FDA.