Arthrex® AR-9215-4CGPPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867239005), received between Aug 5, 2020 and Aug 5, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 16, 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.

• InjuryAug 5, 2020Break; Mechanical Problem

  IT WAS REPORTED THAT DURING A SHOULDER ARTHROPLASTY PROCEDURE, BOTH THE VAULT LOCK MEDIUM PIN GUIDE, AR-9215-4CGPP, AND VAULT LOCK MEDIUM TRIAL, AR-9236-02PP, WERE BROKEN. THE PIN WON'T SLIDE THROUGH PIN HOLE AND THE TRIAL CENTER PEG SNAPPED OFF INSIDE PATIENT. THE PEG WAS REMOVED AND THE CASE WAS COMPLETED WITH NO ADVERSE EFFECT TO THE PATIENT. ADDITIONAL INFORMATION PROVIDED 07/20/2020: THE PEG WAS RETRIEVED; SURGEON HAD TO DRILL AROUND IT TO LOOSEN IT, THEN USED A GRASPER TO RETRIEVE IT. THE SNAPPED OFF PEG WAS LOST AFTER IT WAS RETRIEVED FROM PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10366779 ↗