Ultrasound
RoyalVibe HealthInformation and Alerts
Alert Details
This business has 1 alert.
Ad Review
On September 25, 2021, BBB Serving North Central Texas was alerted to RoyalVibe Health through a consumer inquiry. BBB noted a large number of concerning health claims.
The business appears to be located in a virtual office at 325 N Saint Paul St, STE 3100, Dallas, TX, 75201-3923.
The business advertises on at least two websites: https://royalvibehealth.com & https://www.cellquicken.com
A review indicates the company advertises a non-FDA approved medical device with a "90% cure rate" for various types of cancer and a wide range of different ailments including, but not limited to:
Back Pain
Bradycardia
Cancer
Cataracts
Dementia
Depression
Diabetes
Eye Disease
Heart Disease
Kidney Disease
Kidney Failure
Lung Cancer
Miracle Wellbeing
Neuro-Muscular Disorders
Neuropathy
Neuropsychiatric Disorders
Parkinson's Disease
Post-Traumatic Stress Disorder (PTSD)
Prostate Cancer
Psoriasis
Sinus Conditions
Stage 3 & 4 Cancers
Stroke
BBB contacted the business to seek substantiation or modification for many advertised claims.
According to the BBB Code of Advertising, "Claims relating to performance, energy savings, safety, efficacy or results for a product or service should be based on recent and competent testing or other objective data."
As of October 6, 2021, BBB has received at least one complaint alleging the company told a cancer patient its product was "90% effective" in treating cancer. The consumer was charged $ 4,380 for the device in question.
BBB NCTX recommends strong caution before deciding to purchase products from RoyalVibe Health or CellQuicken.
As of November 5, 2021, the business has failed to respond to BBB requests to substantiate, modify, or discontinue multiple concerning ad claims.
Important Information
Additional Info
On November 18, 2022, the Food & Drug Administration (FDA), sent a Warning Letter to Dr. Raymond L. Venter, CEO of RoyalVibe Health Ltd. The FDA warned Dr. Venter that his business was found to be in violation of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 321(h), for selling adulterated devices intended to diagnose, treat, cure, or prevent many serious health conditions.
The FDA noted the following devices are advertised in violation of the FDA Act: RoyalVibe Bioresonance Focused Ultrasound Generator, Envirovibe Water Restructuring Pad, CellQuicken Analyzer, Therapy Balls Spine Alignment, BrainVibe Neuroplasticity Program, and the RoyalVibe Application.
Additionally, FDA notes that the business "denied and/or limited an inspection of" the company's establishment where the firm's devices are processed, packed, and/or held.
In response to the FDA letter, on July 7, 2022, the business indicated it "will cease offering the RoyalVibe products for sale in the United States" until it complies with FDA regulations.
www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/royalvibe-health-ltd-639553-11182022
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