Arthrex® AR-9592-2420Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867343719), received between Jul 5, 2022 and Jul 5, 2022 — classified as 1 malfunction.

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.

• MalfunctionJul 5, 2022Break

  ON 06/14/2022, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-9625 3.0MM HEX DRIVER AND AN AR-9592-2420 24MM BASEPLATE HAD AN ISSUE, BOTH ITEMS BROKE WHILE BEING USED. THEY WERE RECOVERED AND DISCARDED. THIS WAS DISCOVERED DURING USE ON (B)(6) 2022 WITH NO IMPACT TO THE PATIENT. ADDITIONAL INFORMATION WAS REQUESTED. ON 06/15/2022, THE SALES REPRESENTATIVE REPLIED VIA EMAIL AND STATED THE FOLLOWING INFORMATION: THIS EVENT OCCURRED ON (B)(6) 2022 DURING A REVERSE TOTAL SHOULDER PROCEDURE. THE SALES REPRESENTATIVE PRESENT AT THE CASE WAS BRYSON ELDRIDGE, THE BONE QUALITY OF THE PATIENT WAS NOT PROVIDED, AND NO INSTRUMENT WAS USED TO PREPARE THE BONE SOCKET FOR THE INSERTION OF THE IMPLANTS. THE CASE WAS COMPLETED WITH DIFFERENT INSTRUMENTATION AND THE PATIENT IS FINE TO DATE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14914682 ↗