Arthrex® AR-2923DSRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867239456), received between Jul 12, 2023 and Jul 12, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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 12, 2023Material Fragmentation; Material Fragmentation

  ON (B)(6) 2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN 2.9 MM PUSHLOCK SHAVERDRILL¿, AR-2923DSR, LEFT PLASTIC SHAVINGS INSIDE OF TWO DIFFERENT SHAVER HAND CONTROLS, AR-8330H (SN: (B)(6)) AND AR-8332H (SN: (B)(6)). BOTH SHAVERS APPARENTLY WERE GRINDING THE ATTACHMENTS, AND NOW HAVE PLASTIC SHAVINGS INSIDE, PREVENTING NORMAL USE. NO ADVERSE EVENT OR PATIENT HARM DUE TO THE OUTCOME OF THIS EVENT. PLEASE SEE PICTURES ATTACHED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17304767 ↗