Secret RF Main Unit MTR 2.0 Main UnitRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08800023200171), received between Dec 17, 2025 and Mar 9, 2026 — classified as 2 injuries.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 9, 2026Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS SUBMITTED FOLLOWING PATIENT'S REPORT TO FDA MW5182187. THE PATIENT REPORTED THAT THE TREATMENT OCCURRED ON (B)(6) 2023 AND IDENTIFIED THE DEVICE AS SECRET RF, STATING SHE RECEIVED A SECRET RADIOFREQUENCY TREATMENT THREE TIMES. THE THIRD SECRET RF TREATMENT WAS MUCH MORE PAINFUL AND CAUSED PROLONGED TEARING. AFTER THE SWELLING WENT DOWN, CHEEKS LOOKED FLAT AND THE AREA UNDER EYES APPEARED SUNKEN.

  Patient problems: Deformity/ Disfigurement; Pain

  MAUDE report 24553996 ↗
• InjuryDec 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS REPORT IS SUBMITTED FOLLOWING PATIENT'S REPORT TO FDA MW5178360, CLAIMING "RF MICRONEEDLING SECRET RF AT A DEPTH OF 2 MM ON CHEEKS. IT WAS RECOMMENDED TO ME BC I HAD A SCRATCH ON MY NOSE (32 YRS OLD) LEFT ME WITH FAT LOSS AND FACIAL DISFIGUREMENT. THOUSANDS OF DOLLARS IN TREATMENT TO CORRECT." 1.5 YEAR POST SECRET RF TREATMENT.

  Patient problems: Deformity/ Disfigurement

  MAUDE report 23835104 ↗