Potomac River Group, Corp.: Medical Device Recall in 2021 - (Recall #: Z-0001-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

RAPTAR Laser Range Finders

Product Classification:

Class II

Date Initiated: April 21, 2021

Date Posted: November 3, 2021

Recall Number: Z-0001-2022

Event ID: 88735

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.

Status: Ongoing

Product Quantity: 62 units

Code Information:

RAPTAR G02 (Wilcox Part #57200G02)

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated