Arthrex® AR-2923DSRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867099210), received between May 22, 2024 and Mar 5, 2026 — classified as 2 malfunctions.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 5, 2026Break

  ON 09-FEB-2026, IT WAS REPORTED BY AN ARTHREX SUBSIDIARY EMPLOYEE VIA (B)(4) THAT AN AR-2923DS DISPOSABLES KIT WAS BEING USED TO DRILL THROUGH THE GUIDE WHEN THE GUIDE BROKE IN HALF. THIS OCCURRED DURING USE IN A CASE WITH NO PATIENT EFFECT. THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24518465 ↗
• MalfunctionMay 22, 2024Unintended Movement; Unintended Movement

  IT WAS REPORTED ON 03/28/2023 BY AN ARTHREX EMPLOYEE VIA (B)(4) THAT AN AR-2923DS DISPOSABLES KIT AXIS WAS SHIFTING WHEN USED. UPON CHECKING, BURRS WERE OBSERVED AT THE REAR OF THE DRILL. USED A NEW PRODUCT, AND THE CASE WAS COMPLETED. THIS OCCURRED DURING USE WITH NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19372882 ↗