Schick 100008652Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D0031000086520), received between Jul 7, 2026 and Jul 7, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Communication or Transmission Problem” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 7, 2026Failure to Transmit Record; Communication or Transmission Problem

  WHILE THE CUSTOMER WAS USING A SCHICK33 S2 SENSOR/3.0 CABLE RMA KIT 9', THEY ALLEGE EXPERIENCING IMAGE TRANSMISSION 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 25730769 ↗