Arthrex® AR-8724V-10Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867045576), received between Jan 7, 2020 and Jan 9, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 9, 2020Device Slipped; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT THE SURGEON HAD TO REMOVE THE WRIST SPANNING PLATE, AR-8916SPN, BECAUSE THE SCREWS WERE NOT LOCKED INTO THE DISTAL HOLES. NO FURTHER INFORMATION, ADDITIONAL INFORMATION REQUESTED. ADDITIONAL INFORMATION PROVIDED (B)(6) 2019: CASE DATE OF IMPLANTATION: (B)(6) 2019 CASE DATE OF EXPLANTATION: NOT YET DETERMINED. THE FOLLOWING SCREWS WERE ALSO EXPLANTED DURING THE REVISION: AR-8724-10 LOT: 1058931, AR-8724V-10 LOT: W654331, AR-8724V-16 LOT: W630941, AR-8935-12 LOT: 10220124, AR-8935L-12 LOT: 10248943, AR-8935L-12 LOT: 10257929. NOTE: THE SPECIFIC DATE OF THE SECOND SURGERY (EXPLANT) IS UNKNOWN, HOWEVER IT IS KNOWN THAT THE DATE WAS PRIOR TO 12/4/19. FOR REPORTING PURPOSES (B)(6) 19 HAS BEEN ENTERED AS THE DATE OF EVENT.

  Patient problems: No Information

  MAUDE report 9570033 ↗
• InjuryJan 7, 2020Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE SURGEON HAD TO REMOVE THE WRIST SPANNING PLATE, AR-8916SPN, BECAUSE THE SCREWS WERE BACKING OUT OF THE DISTAL HOLES. NO FURTHER INFORMATION, ADDITIONAL INFORMATION REQUESTED. ADDITIONAL INFORMATION PROVIDED 12/18/2019: CASE DATE OF IMPLANTATION: (B)(6) 2019 CASE DATE OF EXPLANTATION: (B)(6) 2019 THE FOLLOWING SCREWS WERE ALSO EXPLANTED DURING THE REVISION: AR-8916SPN LOT: 105641930, AR-8724-10 LOT: W646301, AR-8724V-10 LOT: 2610171, AR-8724V-12 LOT: W657601, AR-8935-14 LOT: 10279504, AR-8935L-12 LOT: 10257929, AR-8935L-14 LOT: 10277889.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9557191 ↗