ASHLEY BLACK GURU FASCIABLASTER
Received Apr 23, 2019 · Event occurred Dec 1, 2017
Report MW5086163 · MDR key 8550704
Device
Generic name
Massager, Therapeutic, Manual
Manufacturer
Adb Interest, LlcProduct problems
- Break
Patient
38 YR
- Malaise
- Weight Changes
- No Code Available
- Malaise
- Weight Changes
- No Code Available
Narrative
Description of Event or Problem
I BOUGHT THE FASCIABLASTER FROM ASHLEY BLACK COMPANY IN 10/2016, I FOLLOWED HER RECOMMENDED PROTOCOLS AND WATCHED HER VIDEOS, AGAINST ALL ODDS I STARTED FEELING SICK AND GAINED WEIGHT, MY MENSTRUAL PERIOD BECAME CRAZY OUT OF THE CHARTS, SHE CLAIMED IT WAS THE "WORST BEFORE BETTER STAGE" BUT BY LATE (B)(6) I NOTICED A BIG BUMP IN MY BACK, KIND OF LIKE ON TOP OF MY SCAPULA, I GOT IT CHECKED IN (B)(6) 2018 AND IT WAS LIPOMA, I SPOKE WITH MY DOCTOR ABOUT THE BLASTER AND HE THINKS IT COULD BE RELATED TO THAT. I OF COURSE STOPPED USING IT AND TRIED TO SAVE ENOUGH MONEY FOR SURGERY TO REMOVE THE LIPOMA, I STILL CAN'T AFFORD IT. THEN I LEARNED ABOUT ALL THE LEGAL ISSUES MS BLACK IS HAVING, THE FALSE CLAIMS AND THE CONVENIENT (FOR THEM) CHANGES IN THEIR PROTOCOLS. I JUST LEARNED THAT I CAN RETURN THE BLASTER, SINCE IT IS UNDER THE 1000 DAYS GUARANTEE, BUT THEY REFUSE TO GIVE ME A FULL REFUND OF THE (B)(6) DOLLARS I SPEND BUYING THE FASCIABLASTER. I JUST WANT A FULL REFUND FROM THE COMPANY. THE FASCIABLASTER WAS REPLACED BECAUSE IT BROKE BUT THE LAST ONE I RECEIVED BROKE TOO. I AM ATTACHING THE PHOTO. DATE THE PERSON FIRST STARTED TAKING OR USING THE PRODUCT: (B)(6) 2016. DATE THE PERSON STOPPED TAKING OR USING THE PRODUCT: (B)(6) 2017. DID THE PROBLEM STOP AFTER THE PERSON REDUCED THE DOSE OR STOPPED TAKING OR USING THE PRODUCT? FDA SAFETY REPORT ID # (B)(4).