Mighty Patch MP001Recalls & reported problems
Hero Cosmetics, LLC · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00864475000404), received between Oct 28, 2024 and Oct 28, 2024 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Scar Tissue1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS SPONTANEOUS REPORT (B)(4) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER (AGE AND GENDER UNSPECIFIED) WHO NOTICED A PERSISTENT SCAR AND SCAB ON THEIR FACE AFTER USING THE HERO MIGHTY PATCH ORIGINAL. ON AN UNSPECIFIED DATE, THE CONSUMER INITIATED HERO MIGHTY PATCH ORIGINAL TOPICALLY. AFTER TAKING THEM OFF, THE CONSUMER NOTICED IT HAD LEFT A PERSISTENT SCAB AND SCAR ON THEIR FACE AND IT WAS HARD TO COVER WITH MAKEUP. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH HERO MIGHTY PATCH ORIGINAL WAS NOT APPLICABLE. THE OUTCOME OF THE EVENTS WAS NOT RECOVERED.
Patient problems: Scar Tissue
MAUDE report 20543685 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.