Palodent® Plus Sectional Matrix System 659770Recalls & reported problems
Dentsply International Inc. · Palodent Plus Narrow Ring Refill · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 D0026597701), received between Apr 29, 2025 and Apr 29, 2025 — 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.
Reports received per month
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.
MalfunctionApr 29, 2025Break; Break
IN THIS EVENT IT IS REPORTED THAT A PALODENT PLUS NARRW 2 RING RF RING BROKE DURING USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21926368 ↗
Other INSTRUMENTS, DENTAL HAND devices
- Automatrix Snippers+ 62422601Dentsply De Trey GmbH · INSTRUMENTS, DENTAL HAND30 reports
- Palodent® V3 Sectional Matrix System Designed by Triodent® 659760VDentsply International Inc. · INSTRUMENTS, DENTAL HAND27 reports
- AutoMate® 663016Dentsply International Inc. · INSTRUMENTS, DENTAL HAND25 reports
- Automatrix Snippers+ Catch Tray 62422605Dentsply De Trey GmbH · INSTRUMENTS, DENTAL HAND13 reports
- Palodent® V3 Sectional Matrix System Designed by Triodent® 659900VDentsply International Inc. · INSTRUMENTS, DENTAL HAND9 reports
- Palodent® V3 Sectional Matrix System Designed by Triodent® 659770VDentsply International Inc. · INSTRUMENTS, DENTAL HAND7 reports
- Palodent® Plus Sectional Matrix System 659760Dentsply International Inc. · INSTRUMENTS, DENTAL HAND7 reports
- AutoMate® 663100Dentsply International Inc. · INSTRUMENTS, DENTAL HAND5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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