Schick 100008624Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI D0031000086240), received between Feb 11, 2026 and Mar 23, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (8 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 8 most recent of 8 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, THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24660951 ↗
• MalfunctionFeb 24, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', 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 24430332 ↗
• MalfunctionFeb 17, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', 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 24367330 ↗
• MalfunctionFeb 17, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', 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 24366943 ↗
• MalfunctionFeb 11, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', 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 24314777 ↗
• MalfunctionFeb 11, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', THEY ALLEGE THERE WAS AN X-RAY IMAGE TRANSMISSION ISSUE WHERE THE X-RAY IMAGE WAS NOT CAPTURED AFTER RADIATION HAS OCCURRED (TRANSMISSION FAILURE). NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24314744 ↗
• MalfunctionFeb 11, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, 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 24312372 ↗
• MalfunctionFeb 11, 2026Poor Quality Image

  WHILE THE CUSTOMER WAS USING A PART OF AN INTRAORAL SENSOR SYSTEM, SCHICK33 S2 SENSOR SHIP KIT/3.0 CABLE 6', 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 24312347 ↗