Medical device recalls Moderate risk

Potomac River Group, Corp. recalls RAPTAR Laser Range Finders

Recall date
April 21, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0001-2022
FDA classification
Class II
Brand / firm
Potomac River Group, Corp.
Sold / distributed
US Nationwide

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

RAPTAR Laser Range Finders

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