Schick/XIOS AE 100008286Recalls & reported problems
Sirona Dental, Inc. · Schick 3.0 USB Interface · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI D7641000082861), received between Aug 10, 2023 and Oct 3, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Image Display Error/Artifact” (3 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Image Display Error/Artifact3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 3, 2023Image Display Error/Artifact; Image Display Error/Artifact
WHILE USING A SCHICK 33 SENSOR INTRAORAL X-RAY UNIT, AN INCORRECT IMAGE WAS DISPLAYED DURING USE. THIS WAS IMMEDIATELY NOTICEABLE TO THE CLINICIAN AND NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17860253 ↗MalfunctionAug 10, 2023Image Display Error/Artifact; Image Display Error/Artifact
WHILE USING A SCHICK 33 SENSOR INTRAORAL X-RAY UNIT, AN INCORRECT IMAGE WAS DISPLAYED DURING USE. THIS WAS IMMEDIATELY NOTICEABLE TO THE CLINICIAN AND NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17503124 ↗MalfunctionAug 10, 2023Image Display Error/Artifact; Image Display Error/Artifact
WHILE USING A SCHICK 33 SENSOR INTRAORAL X-RAY UNIT, AN INCORRECT IMAGE WAS DISPLAYED DURING USE. THIS WAS IMMEDIATELY NOTICEABLE TO THE CLINICIAN AND NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17503048 ↗
Other Unit, X-Ray, Extraoral With Timer devices
- DIOX-602 1DigiMed Co., Ltd. · Unit, X-Ray, Extraoral With Timer1 recall0 reports
- Panoramic Corporation PC-1000Young Ps Acquisition, LLC · Unit, X-Ray, Extraoral With Timer7 reports
- Panoramic Corporation PC-1000/Laser 1000Young Ps Acquisition, LLC · Unit, X-Ray, Extraoral With Timer5 reports
- Schick AE 100006036Sirona Dental, Inc. · Unit, X-Ray, Extraoral With Timer1 report
- Panoramic Corporation PC-4000Young Ps Acquisition, LLC · Unit, X-Ray, Extraoral With Timer1 report
- Panoramic Corporation CCD EncompassYoung Ps Acquisition, LLC · Unit, X-Ray, Extraoral With Timer1 report
- FocusPaloDEx Group Oy · Unit, X-Ray, Extraoral With Timer1 report
- CS 2200Carestream Dental LLC · UNIT, X-RAY, EXTRAORAL WITH TIMER1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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