J-PLASMA® PRECISE™ BVX-150BRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00607151010140), received between Jul 24, 2018 and Jan 22, 2020 — classified as 5 injuries.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K151325); they may or may not involve this specific model.

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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryJan 22, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  PATIENT RECEIVED A SUBMENTAL BURN AFTER A LIPOSUCTION PROCEDURE FOLLOWED BY RENUVION.

  Patient problems: Burn(s); Injury

  MAUDE report 9615863 ↗
• InjuryJan 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT HAD PNEUMOTHORAX AFTER A J-PLASMA PROCEDURE ON NECK, ARMS AND ABDOMEN.

  Patient problems: Patient Problem/Medical Problem; Pneumothorax

  MAUDE report 9574243 ↗
• InjuryMay 15, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  COMPLAINT FOR A SUBCUTANEOUS HEMATOMA ON LEFT CHEST AFTER SURGERY. ASPIRATION PERFORMED WITH NO RETURN OF FLUID.

  Patient problems: Bruise/Contusion; Hematoma; Injury

  MAUDE report 8612136 ↗
• InjuryJul 24, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

  COMPLAINT ALLEGED THAT THE PATIENT RECEIVED A BURN IN THE INCISION SITES RIGHT AND LEFT LOWER ABDOMINAL AREA AND BELLY BUTTON AFTER A J-PLASMA PROCEDURE.

  Patient problems: Partial thickness (Second Degree) Burn

  MAUDE report 7716415 ↗
• InjuryJul 24, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

  COMPLAINT ALLEGED THAT THE PATIENT RECEIVED A BURN IN THE LEFT ELBOW IN THE INCISION SITE DURING A PROCEDURE.

  Patient problems: Partial thickness (Second Degree) Burn

  MAUDE report 7716405 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K151325. One submission often covers many models, so check the product and lot details in each record.

• Z-2061-2020 · Apr 20, 2020 · Terminated
  Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B, BVX-270B, BVX-330B, BVX-270BPP, BVX- 330BPS, APYX-150B, APYX-270B, APYX-330B, APYX- 270BPP, and APYX-330BPS. P