Arthrex® AR-300-044SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867028289), received between Dec 27, 2024 and Dec 27, 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 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.

• MalfunctionDec 27, 2024Break; Break

  IT WAS REPORTED THAT DURING A KNEE ARTHROSCOPY THE DEVICE BROKE. PER COMPLAINT REPORTER THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A NEW DEVICE WITH THE SAME PART NUMBER. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY. UPDATE AVOE 04-DEC-2024 IT WAS CONFIRMED THAT NO PART OF THE DEVICE BROKE. THE DEVICE DIDN`T WORK DURING SURGERY. UPDATE AVOE 17-DEC-2024 SINCE THE DESCRIPTION "DIDN`T WORK" IS NOT REALLY APPLICABLE FOR A SAW BLADE, WHICH IS AFFECTED IN THIS CASE, FURTHER QUESTIONS WERE ASKED. FURTHER INFORMATION WAS PROVIDED THAT THE DEVICE INDEED BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21025715 ↗