Viant Medical, LLC T2776Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840096405873), received between Mar 28, 2024 and Mar 28, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• MalfunctionMar 28, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED DURING A PROCEDURE ON THE RIGHT SIDE OF THE PATIENT THAT WHILE REAMING, THE REAMED SPACE APPEARED TOO LARGE FOR THE CUPS. THE SURGEON ATTEMPTED TO IMPLANT A SIZE 56MM CUP USING THE SIZE 55MM REAMER (THIS REPORT). THE SURGEON THEN ATTEMPTED TO IMPLANT A SIZE 58MM CUP USING THE 57MM REAMER (REPORT 3004976965-2024-00007). A SCREW WAS USED TO TRY AND IMPLANT ONE OF THE CUPS, BUT THERE STILL DID NOT SEEM TO BE GOOD FIXATION. BOTH SIZE 56MM AND 58MM CUPS WERE WASTED. A SIZE 60MM CUP WAS ULTIMATELY IMPLANTED AND THE SURGEON DID NOT HAVE TO REAM ANY ADDITIONAL BONE. THERE WAS SURGICAL DELAY OF ABOUT 30 MINUTE WITH NO CONSEQUENCES OR IMPACT TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19000462 ↗