Arthrex® AR-9228GRPPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867239074), received between Apr 30, 2024 and Apr 30, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Dull, Blunt” (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.

• MalfunctionApr 30, 2024Dull, Blunt; Dull, Blunt

  ON 10/20/2021, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA PHONE THAT THE FOLLOWING REAMERS WERE FOUND TO BE DULL: AR-9288GRPP, AR-9229GRPP, AR-9230GRPP AND AR-9231GRPP. THE SURGEON USED ALL REAMERS, FROM SMALLEST (AR-9288GRPP) TO LARGEST (AR-9231GRPP) UNTIL THE DEPTH DESIRED FOR EACH WAS REACHED. AFTER COMPLETION WITH THE EXTRA-LARGE REAMER, THE SURGEON WENT BACK TO THE SMALL REAMER AND BEGAN TO REAM THE INSERTION SITE. DURING REAMING THE SURGEON USED FORCE ON THE SMALL REAMER CAUSING THE DEVICE TO REAM MORE THAN THE DESIRED DEPTH ON THE GLENOID. THIS PORTION OF THE PROCEDURE WAS COMPLETED USING EXTRA CEMENT TO ACHIEVE GOOD FIXATION

  Patient problems: Insufficient Information

  MAUDE report 19212239 ↗