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Cavitron® 8161428Recalls & reported problems

Dentsply Professional · Cavitron® Jet Plus Ultrasonic Scaling System Package. Contains: 1 Cavitron Jet Plus Ultrasonic Scaler and Air Polishing System, 3 Jet-Mate® Sterilizable Detachable Handpieces, 2 Jet Air Polishing Inserts, 1 Prophy-Jet® Sodium Bicarbonate Powder 13 Oz. Bottle, 1 Jet-Fresh® Aluminum Trihydroxide Prophy Powder 13 Oz. Bottle, 1 30K Focused Spray® SlimLINE® 10S Ultrasonic Insert - FitGrip® · Class 2

Adverse event reports
13
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI D00381614281), received between May 22, 2023 and May 1, 2026 — classified as 13 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (8 reports).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 1 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 1 reportsMay 2024: 1 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 3 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 1 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 1 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Overheating of Device8
  • Restricted Flow rate5
  • No Flow4

Patient problems

  • No Clinical Signs, Symptoms or Conditions13

Recent adverse event reports

The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 1, 2026Restricted Flow rate

    WHILE USING A CAVITRON JET PLUS G137, THEY ALLEGE THAT THEY HAVE LOW WATER FLOW AND THE HANDPIECE IS HEATING UP, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25056935 ↗
  • MalfunctionDec 16, 2025Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT A CAVITRON JET PLUS PACKAGE-2015 IS ALLEGED TO OVERHEATED AND THE INSERTS GOT HOT DURING USE. NO INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23819373 ↗
  • MalfunctionAug 13, 2025No Flow; No Flow

    WHILE USING A STERI-MATE THEY ALLEGE THAT THEY HAVE NO WATER FLOW OR VIBRATION AND THE INSERT TIPS ARE HEATING UP, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22793885 ↗
  • MalfunctionFeb 6, 2025No Flow; No Flow

    WHILE USING A STERI-MATE 30K HANDPIECE, THEY ALLEGE THAT THEY HAVE NO WATER FLOW AND THE HANDPIECE IS HEATING UP, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21324034 ↗
  • MalfunctionSep 25, 2024Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT CAVITRON JET PLUS PACKAGE-2015 ALLEGED THAT OVERHEATED AND THE TIP GETS HOT. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20300574 ↗
  • MalfunctionSep 25, 2024Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT CAVITRON JET PLUS PACKAGE-2015 IT IS ALLEGED TO HAVE OVERHEATED AND TIP GOT HOT. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20300518 ↗
  • MalfunctionSep 25, 2024Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT CAVITRON JET PLUS PACKAGE-2015 IS ALLEGED THAT OVERHEATED AND THE TIP GETS HOT. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20300442 ↗
  • MalfunctionJun 19, 2024Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT CAVITRON JET PLUS PACKAGE-2015 WHILE USED BEING USED IT IS ALLEGED THAT THE INSERT GOT HOT. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19566510 ↗
  • MalfunctionMay 23, 2024Restricted Flow rate; No Flow; Restricted Flow rate; No Flow

    WHILE USING A CAVITRON JET PLUS G137 THEY ALLEGE THAT THEY ARE NOT GETTING ENOUGH WATER TO THE HANDPIECE AND THE HANDPIECE AND INSERTS ARE GETTING WARM, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19381182 ↗
  • MalfunctionApr 19, 2024Restricted Flow rate; Restricted Flow rate

    WHILE USING A CAVITRON JET PLUS G137 THEY ALLEGE THAT LOW WATER FLOW TO HANDPIECE AND HANDPIECE IS GETTING HOT; NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19149596 ↗
  • MalfunctionFeb 14, 2024Restricted Flow rate; Overheating of Device; Restricted Flow rate; Overheating of Device

    WHILE USING A CAVITRON JET PLUS G137, THEY ALLEGE THAT THE INSERTS ARE GETTING HOT WITH POTENTIAL WATER FLOW ISSUE, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18707451 ↗
  • MalfunctionJan 23, 2024Restricted Flow rate; Overheating of Device; No Flow; Restricted Flow rate; Overheating of Device; No Flow

    WHILE USING A CAVITRON JET PLUS G137, THEY ALLEGE THAT THEY HAVE MINIMAL WATER AND THE HANDPIECE IS HEATING UP, NO INJURY RESULTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18564643 ↗
  • MalfunctionMay 22, 2023Overheating of Device; Overheating of Device

    IN THIS EVENT IT IS REPORTED THAT CAVITRON JET PLUS PACKAGE-2015 ALLEGEDLY IS HEATING UP DUE TO LACK OF WATER FLOW. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16973595 ↗

Other Scaler, ultrasonic devices

All Scaler, ultrasonic devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.