Cavitron® 81872Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI D003818721), received between Jun 9, 2025 and Dec 16, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “No Flow” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 16, 2025Overheating of Device; Overheating of Device

  WHILE THE CUSTOMER WAS USING A CAVITRON JET PLUS G137 THEY ALLEGE THAT THE INSERT IS OVERHEATING. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23817577 ↗
• MalfunctionDec 16, 2025No Flow; No Flow

  WHILE USING A CAVITRON JET PLUS G137, THEY ALLEGE THAT THEY HAVE LOW TO NO WATER FLOW AND THE HANDPIECE GOT HOT. NO INJURY RESULTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23817575 ↗
• MalfunctionJun 9, 2025Restricted Flow rate; Restricted Flow rate

  WHILE USING A CAVITRON JET PLUS G137, THEY ALLEGE THAT THEY HAVE LOW WATER FLOW AND THE HANDPIECE GETS WARM TO THE TOUCH; NO INJURY RESULTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22165848 ↗