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Schick33 100008633Recalls & reported problems

Sirona Dental, Inc. · SCHICK33 S2 SENSOR STARTER KIT/3.0 INTERFACE, 6' · Class 2

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI D764100008633), received between Aug 10, 2023 and Sep 13, 2023 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Image Display Error/Artifact” (4 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Image Display Error/Artifact4

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 13, 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 17736321 ↗
  • 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 17502955 ↗
  • 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 17502954 ↗
  • 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 17502945 ↗

Other Solid State X-Ray Imager (Flat Panel/Digital Imager) devices

All Solid State X-Ray Imager (Flat Panel/Digital Imager) devices →

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