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Renuvion®/J-Plasma® APYX-150-BPPRecalls & reported problems

Apyx Medical Corporation · Renuvion®/J-Plasma Precise® Open 150mm · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00607151050047), received between Nov 11, 2020 and Nov 11, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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

Device problems

  • Use of Device Problem1
  • Use of Incorrect Control/Treatment Settings1

Patient problems

  • Erythema1
  • Hypersensitivity/Allergic reaction1
  • Local Reaction1
  • Skin Discoloration1
  • Subcutaneous Nodule1

Recent adverse event reports

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

  • InjuryNov 11, 2020Use of Incorrect Control/Treatment Settings; Use of Device Problem; Use of Incorrect Control/Treatment Settings; Use of Device Problem

    PATIENT PRESENTED 10 DAYS POST OPERATIVE WITH NODULES AND ERYTHEMA. THE INVESTIGATION CONCLUDED THAT THE ISSUE IS ASSOCIATED WITH POOR SURGICAL TECHNIQUE. THERE WAS NO REPORTED MALFUNCTION OF THE DEVICE.

    Patient problems: Erythema; Hypersensitivity/Allergic reaction; Local Reaction; Skin Discoloration; Subcutaneous Nodule

    MAUDE report 10822301 ↗

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page