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Open, Classified

RAPTAR Laser Range Finders

FDA Recall Z-0001-2022 · Posted None

Recalling FirmPotomac River Group, Corp.
Recall StatusOpen, Classified
Product CodeREP
Date Initiated2021-04-21
Product Quantity62 units

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.

Firm Action

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.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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