Truliant 02-022-55-3525Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862317155), received between Jul 9, 2026 and Jul 9, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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.

• InjuryJul 9, 2026Loss of Osseointegration

  REPORT #2 OF 2 FOR THIS EVENT. AS REPORTED, A PATIENT HAD A LEFT TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, ONE (1) YEAR, SEVEN (7) MONTHS LATER, THE PATIENT UNDERWENT A LEFT KNEE REVISION DUE TO INADEQUATE OSTEOINTEGRATION OF THE POROUS COMPONENTS. AS A RESULT, THE PATIENT WAS REVISED TO CEMENTED COMPONENTS. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO ADDITIONAL MEDICAL OR CLINICAL INFORMATION WAS PROVIDED. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 25761438 ↗