Cannulated Screws 71101044Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010437310), received between Mar 31, 2020 and Mar 31, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjuryMar 31, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT DURING SURGERY, THE SURGEON PROCEEDED TO INSERT THE 4.0MM CANNULATED SCREW AND WHEN INSERTING THE SCREW, IT WAS FOUND THAT THE SCREW WAS NOT GOING IN, THEREFORE THE SURGEON DECIDED TO CHECK ON THE X-RAY IMAGE INTENSIFIER. IT WAS FOUND THAT THE GUIDEWIRE WENT DEEPER AND THE SCREW WAS THE ONE PUSHING THE GUIDEWIRE IN. HE TOOK OUT THE CANNULATED SCREW AND TESTED WITH ANOTHER GUIDEWIRE BEFORE ANOTHER ATTEMPT. WE FOUND THAT ALL THE GUIDEWIRE COULDN¿T GO THROUGH THE PARTICULAR CANNULATED SCREW.

  Patient problems: Injury

  MAUDE report 9902763 ↗