EXPEDIUM 310002150PRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034469485), received between Mar 13, 2024 and Mar 13, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• MalfunctionMar 13, 2024Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

  IT WAS REPORTED THAT ON FEBRUARY 26 2024, THE SCREWDRIVER DISTAL END TIP WAS STRIPPED AND THE SLEEVE NO LONGER ENGAGED WITH THE SCREW HEAD CORRECTLY. THE PATIENT WAS NOT IMPACTED AS A NEW SCREWDRIVER FROM ANOTHER SET WAS USED. THERE WAS NO DELAY IN SURGERY. THIS REPORT IS FOR ONE PWR XPDM POLY DRIVER, HANDLE THIS IS REPORT 1 OF 3 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18895527 ↗