Skip to content

SCHICK33 B1218000Recalls & reported problems

Sirona Dental, Inc. · SCHICK33 S2 SENSOR SHIP KIT 6 FT · 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 D764B12180001), received between Aug 10, 2023 and Aug 10, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Image Display Error/Artifact” (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.

Most reported problems

Device problems

  • Image Display Error/Artifact1

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.

  • 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 17503125 ↗

Other Unit, X-Ray, Intraoral devices

All Unit, X-Ray, Intraoral devices →

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