Schick 100008290Recalls & reported problems
Dentsply International Inc. · SCHICK 33 USB 3.0 Package, RMA · 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 D0031000082900), received between Feb 24, 2026 and Feb 24, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Poor Quality Image” (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
- Poor Quality Image1
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.
MalfunctionFeb 24, 2026Poor Quality Image
WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24430305 ↗
Other Unit, x-ray, intraoral devices
- Schick B1218000Dentsply International Inc. · Unit, x-ray, intraoral4 reports
- Schick 100008720Dentsply International Inc. · Unit, x-ray, intraoral2 reports
- Schick33 100008660Sirona Dental, Inc. · Unit, X-Ray, Intraoral2 reports
- Xios XG Supreme 6724723Dentsply International Inc. · Unit, x-ray, intraoral1 report
- Schick 100008652Dentsply International Inc. · Unit, x-ray, intraoral1 report
- SCHICK33 B1218200Sirona Dental, Inc. · Unit, X-Ray, Intraoral1 report
- SCHICK33 B1218000Sirona Dental, Inc. · Unit, X-Ray, Intraoral1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.