Arthrex® AR-8610D-30Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867197275), received between Aug 18, 2022 and Aug 18, 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 18, 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.

• MalfunctionAug 18, 2022Break

  IT WAS REPORTED THAT DURING A SURGERY FOUR DRIVERS BROKE DURING REMOVAL OF THE SCREW. NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY WAS REPORTED. UPDATE (B)(6) 2022: REMOVAL OF PLATE AND SCREWS WAS PERFORMED. THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD-PARTY. ANOTHER SCREW DRIVER WAS USED TO FINISH THE SURGERY SUCCESSFULLY. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY. UPDATE (B)(6) 2022: THE PART AND LOT NUMBERS OF BROKEN DRIVERS WERE RECEIVED: AR-8610D-25, LOT 6045184103 AR-8737-25, LOT 01391809 AR-8610D-30, LOT (10)1392150 AR-8737-26, LOT (10)1392118

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15249447 ↗