Potomac River Group, Corp. RAPTAR Laser Range Finders Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RAPTAR Laser Range Finders
Brand
Potomac River Group, Corp.
Lot Codes / Batch Numbers
RAPTAR G02 (Wilcox Part #57200G02)
Products Sold
RAPTAR G02 (Wilcox Part #57200G02)
Potomac River Group, Corp. is recalling RAPTAR Laser Range Finders due to 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.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Potomac River Group (PRG) sent communications to the purchasers of the affected units that were locked in the eye safe mode and distributed without the keys. PRG expects to offer all affected purchasers at least a refund option. PRG s ability to offer a repair option is contingent upon assistance from Wilcox, which is the only entity PRG is aware of that has the ability to render the units compliant with FDA specifications.
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