Medical device recalls Moderate risk

p-Chip Corporation recalls p-Chip Wand Reader

Recall date
March 3, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1693-2023
FDA classification
Class II
Brand / firm
p-Chip Corporation
Sold / distributed
US Nationwide Distribution

Why it was recalled

The laser operation might fall under a higher laser class.

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

What was recalled

p-Chip Wand Reader

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