Schick B1218051Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI D003B12180510), received between Mar 4, 2026 and May 6, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 6, 2026Intermittent Communication Failure

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, THEY ALLEGE EXPERIENCING CONNECTIVITY ISSUES WHEN AN X-RAY IMAGE WAS TAKEN OR AN ADDITIONAL IMAGE WAS REQUIRED. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25092775 ↗
• MalfunctionMar 4, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR RMA KIT, 6FT, THEY ALLEGE THE DEVICE SELF TRIGGERED, CAUSING AN X-RAY IMAGE TO BE TAKEN WITHOUT PROMPTING THE DEVICE TO TAKE AN IMAGE. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24506658 ↗
• MalfunctionMar 4, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR RMA KIT, 6FT, THEY ALLEGE THERE WAS A DEVICE RESPONSE ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (NO DEVICE OUTPUT). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24506621 ↗