T7Plus 0416-831-200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327465907), received between Jun 5, 2024 and Jun 5, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unraveled Material” (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, 2024Unraveled Material; Unraveled Material

  IT WAS REPORTED THAT WHILE CLOSING DURING A TOTAL KNEE PROCEDURE AT THE USER FACILITY FIBERS FROM DEVICE WAS FOUND ON THE JOINT AND HAD TO RE IRRIGATE THE KNEE TO FLUSH THE FIBERS OUT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT A CLINICALLY SIGNIFICANT DELAY; NO MEDICAL INTERVENTION OR ADVERSE CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19473404 ↗