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Cavitron® 79611Recalls & reported problems

Dentsply Professional · Slimline® Ultrasonic Insert 30K SLI® 10S · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D003796111), received between Mar 13, 2023 and Mar 13, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

Device problems

  • Break1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

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

  • MalfunctionMar 13, 2023Break; Break

    IN THIS EVENT IT IS REPORTED THAT A 30K SLI-10S INSERT,PACKED TIP BROKE DURING USE AND WAS INGESTED BY THE PATIENT. THE DOCTOR INITIALLY TOLD THE PATIENT THAT IT WOULD PASS BUT THE PATIENT CHOSE TO HAVE SURGERY TO HAVE THE TIP REMOVED. IT¿S UNCLEAR IF THE SURGERY WAS NECESSARY.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 16532282 ↗

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.