Truliant, Activit-E 02-024-35-5009Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862597342), received between Jul 1, 2026 and Jul 1, 2026 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K223252); they may or may not involve this specific model.

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.

• InjuryJul 1, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THIS PATIENT UNDERWENT A LEFT KNEE REPLACEMENT. SUBSEQUENTLY, THEY DEVELOPED AN INFECTION. THE SURGEON WASHED OUT THE JOINT AND EXCHANGED THE POLY. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Unspecified Infection

  MAUDE report 25680627 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K223252. One submission often covers many models, so check the product and lot details in each record.

• Z-0586-2024 · Nov 21, 2023 · Open, Classified
  Exactech Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032, c) 02-023-02-0035, d) 02-023-02-0038, e) 02-024-35-1512, f) 02-024-35-1515,