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Palodent® V3 Sectional Matrix System 659700VRecalls & reported problems

Dentsply International Inc. · Palodent® V3 Introductory Kit · Class 1

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 D002659700V1), received between Jun 20, 2023 and Jun 20, 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

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 20, 2023Break; Break

    IN THIS EVENT IT IS REPORTED THAT PALODENT V3 STARTER KIT BROKE DURING USE. NO INJURY OCCURRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17163514 ↗

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