Automatrix Snippers+ Catch Tray 62422605Recalls & reported problems
Dentsply De Trey GmbH · Automatrix Snippers+ Catch Tray is a part of the Automatrix Snippers+ to prevent clipped loop pieces rom the oral cavity. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 D010624226051), received between Nov 3, 2025 and Jun 10, 2026 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Break” (13 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break13
Patient problems
- No Clinical Signs, Symptoms or Conditions12
- Insufficient Information5
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. ALL THE BROKEN PARTS WERE RETRIEVED FROM THE PATIENT'S MOUTH. NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25461450 ↗MalfunctionMay 12, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25150734 ↗MalfunctionApr 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25049007 ↗MalfunctionApr 17, 2026Break
IN THIS EVENT IT WAS REPORTED THAT AN AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24913324 ↗MalfunctionApr 17, 2026Break
IN THIS EVENT IT WAS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24913269 ↗MalfunctionApr 17, 2026Break
IN THIS EVENT IT WAS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24913177 ↗MalfunctionMar 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATE III BROKE DURING USE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24732168 ↗MalfunctionMar 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information
MAUDE report 24731903 ↗MalfunctionMar 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24729818 ↗MalfunctionMar 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT BROKE DURING USE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24729726 ↗MalfunctionMar 30, 2026Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX BROKE DURING USE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24713656 ↗MalfunctionDec 22, 2025Break; Break
IN THIS EVENT IT IS REPORTED THAT AN AUTOMATRIX SHAFT BROKE DURING USE. NO INJURY OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23862940 ↗MalfunctionNov 3, 2025Break; Break
IN THIS EVENT IT IS REPORTED THAT A AUTOMATRIX SHAFT - AUTOMATRIX TIGHTENING DEVICE BROKE DURING USE. NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23450116 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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