FDAAugust 30, 2023device

CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe Therapy Balls

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of customers' reliance on marketing claims which could cause the user to forgo medical treatment resulting in health consequences.

What to do

FDA enforcement status: Ongoing

Brands named

royalvibe healthroyalvibe

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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