SCHICK33 B1309001Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI D764B13090011), received between Jun 3, 2026 and Jun 4, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Patient Data Problem” (2 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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 4, 2026Patient Data Problem

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE A PREVIOUS PATIENT¿S X-RAY IMAGE WAS TRANSFERRED INSTEAD OF THE CURRENT PATIENT. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25390785 ↗
• MalfunctionJun 3, 2026Patient Data Problem

  WHILE THE CUSTOMER WAS USING A SCHICK33 SENSOR SHIP KIT S0, 9FT, THEY ALLEGE A PREVIOUS PATIENT'S X-RAY IMAGE WAS TRANSFERRED INSTEAD OF THE CURRENT PATIENT. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25373390 ↗