Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CellQuicken Analyzer (Smart-Watch and Software) Recalled by RoyalVibe Health Ltd. Due to Ultrasound devices were not authorized, cleared, or approved...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact RoyalVibe Health Ltd. directly.
Affected Products
CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe Therapy Balls
Quantity: 564
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 38 states: AL, AZ, CA, CO, CT, FL, GA, HI, IL, IN, IA, KY, LA, ME, MD, MA, MI, MN, MS, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, WA, WI, DC
About RoyalVibe Health Ltd.
RoyalVibe Health Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report