Schick 100008286Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI D0031000082860), received between Feb 18, 2026 and Mar 23, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (5 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 23, 2026Poor Quality Image

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24661698 ↗
• MalfunctionFeb 24, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, 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 24430996 ↗
• MalfunctionFeb 19, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, 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 24387944 ↗
• MalfunctionFeb 19, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, 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 24387579 ↗
• MalfunctionFeb 18, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK AE USB INTERFACE, 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 24377046 ↗