Arthrex® AR-1209LRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867005082), received between Jun 5, 2024 and Jun 5, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Corroded” (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.

• MalfunctionJun 5, 2024Corroded; Corroded

  IT WAS REPORTED THAT AFTER THE FIRST TIME IN THE STERILIZER, THERE IS IMMEDIATELY STRONG DISCOLORATION AND SOME MARKINGS HAVE ALREADY DISAPPEARED. THERE WAS NO HARM OR ADVERSE EVENT FOR PATIENT, OPERATOR OR THIRD PARTY REPORTED. NO FURTHER INFORMATION RECEIVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19473227 ↗