Medical device recalls Moderate risk

Visionsense, Ltd. recalls VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS) - 785nm Product Number: 175-0012

Recall date
October 17, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0281-2023
FDA classification
Class II
Brand / firm
Visionsense, Ltd.
Sold / distributed
US Nationwide distribution.

Why it was recalled

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

What was recalled

VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS) - 785nm Product Number: 175-0012

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