inforMED
MalfunctionFMP

D'OXYVA - CIRCULARITY HEALTHCARE CO2 TREATMENT

Received Oct 8, 2021 · Event occurred Jul 20, 2021

Report MW5104515 · MDR key 12615575

Device

Generic name

Protector, Skin Pressure

Product problems

  • Nonstandard Device
  • Defective Device

Patient

Not reported

  • Insufficient Information
  • Insufficient Information

Narrative

Description of Event or Problem

D'OXYVA - CIRCULARITY HEALTHCARE CO2 TREATMENT, CO2 DEVICE, NON-INVASIVE TRANSDERMAL DELIVERY SYSTEM. (B)(6) THEIR COMPANY CLAIMS ITS PRODUCTS ARE LIFE SAVING AND REGENERATIVE, EVEN IN GRAVE HEALTH CRISIS. THE WAND CARTRIDGES, WHICH CONTAIN CONTENTS UNDER PRESSURE, ARE HIGHLY VOLATILE AND PROMOTE RISK OF INJURY. AT LEAST ONE ASPECT OF THEIR INITIAL WAND WAS RECALLED AND REPLACED, DUE TO DEFECT. THEY CONTINUE TO FINANCIALLY EXPLOIT UNSUSPECTING, DESPERATELY ILL AND DYING PATIENTS WITH THEIR ONGOING SCAM. THIS COMPANY CONTINUES TO FINANCIALLY ABUSE AND PHYSICALLY INJURE CONSUMERS. FDA SAFETY REPORT ID# (B)(4).