Vanguard® Vivacit-E® VE183560Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024565401), received between Jan 12, 2021 and Jan 12, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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.

• MalfunctionJan 12, 2021Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING RIGHT TOTAL KNEE ARTHROPLASTY THE LOCKING CLIP WAS DIFFICULT TO INSERT THROUGH THE TIBIAL INSERT AND TIBIAL TRAY. A SECOND TIBIAL INSERT AND LOCKING CLIP WERE USED TO COMPLETE THE PROCEDURE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE AT THIS TIME.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 11154693 ↗