Arthrex® AR-11600NRFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867273047), received between Oct 24, 2024 and Oct 24, 2024 — 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.

• MalfunctionOct 24, 2024Break; Break

  IT WAS REPORTED THAT THE DEVICE IS DEFECTIVE. ALSO, THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY REPORTED. IT WILL BE PROCESSED AS REPAIR, NOT AS COMPLAINT. UPDATE (B)(6) 18-OCT-2024: FURTHER INFORMATION WAS PROVIDED THAT DURING THE REPORTED EVENT HAS OCCURRED DURING A SURGERY. THE SURGEON TRIED TO REMOVE A FREE JOINT BODY FROM THE JOINT. THE FORCEPS BROKE OFF DURING THE FIRST ATTEMPT. UPDATE (B)(6) 24-OCT-2024: FURTHER INFORMATION WAS PROVIDED THAT THE SHEAR PIN INSIDE THE HANDLE BROKE OUTSIDE THE PATIENT. THE REPORTED EVENT OCCURRED DURING A KNEE ARTHROSCOPY WITH ANTERIOR CRUCIATE LIGAMENT PLASTIC. PER COMPLAINT REPORTER THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A DIFFERENT PLIER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20522669 ↗