FDA recall record

RoyalVibe Health CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound recall — FDA Z-0082-2024

Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established.…

Class IIclassification
Z-0082-2024official record ID
Oct 18, 2023report date

Recall record at a glance

Official recordZ-0082-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRoyalVibe Health Ltd.
Report dateOct 18, 2023
Recall initiation dateAug 30, 2023
Quantity564
LocationThe Woodlands, TX, United States

Official product description

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

Why the product was 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.

Distribution information

US: MI, PA, TX, GA, OH, CA, FL, NY, NH, UT, AL, WA. WI, MN, MA, NM, IA, MD, IL, SC, NJ, NC, NV, TN, AZ, OR, OK, LA, OR, NE, ME, CO, MS, MT, CT, KY, HI, IN, DC

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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