InMode RF hand piece HP172246ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07290016633405), received between May 18, 2023 and May 18, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).

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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 18, 2023Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

  2 FULL-THICKNESS BURNS (3RD DEGREE) OF OVAL SHAPE ABOUT 1 CM IN DIAMETER EACH. ANATOMICAL LOCATION NOT CLEAR IN THE PHOTO, PRESUMABLY ON THE RIGHT SIDE OF THE ABDOMEN. ONE OF THE LESIONS APPEARS DEVOID OF DERMAL TISSUE WHILE THE OTHER HAS A NECROTIC BLACK CRUST. THE WOUNDS REQUIRE PROPHYLACTIC MEDICAL CARE IN ORDER TO PREVENT SECONDARY INFECTION AND TO BOOST THE HEALING PROCESS. AT THE MOMENT, SCAR FORMATIONS IN CORRESPONDENCE WITH THE LESIONS CANNOT BE EXCLUDED.STILL AWAITING FURTHER DETAILS FROM THE CLINIC.

  Patient problems: Full thickness (Third Degree) Burn

  MAUDE report 16952371 ↗