EXPEDIUM VERSE 299704152PRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034501437), received between Apr 29, 2022 and Apr 29, 2022 — 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.

• MalfunctionApr 29, 2022Device-Device Incompatibility; Device-Device Incompatibility

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT WHILE A REP WAS MAKING A DEMONSTRATION PRIOR TO SURGERY FOR A SURGEON WITH THE EXPEDIUM VERSE NAVIGATION SYSTEM ON (B)(6) 2022, TWO KINDS OF SHAFTS WERE NOT ABLE TO BE ATTACHED TO THE DRIVER HANDLE IN QUESTION. IT WAS FINALLY CONFIRMED THAT THE DRIVER HANDLE IN QUESTION TRIGGERED THE EVENT.. NO PATIENT INVOLVEMENT. THIS COMPLAINT INVOLVES ONE (1) DEVICE VERSE POLY DRIVER HANDLE PWR. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14253506 ↗