Exactech 170-36-03Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862155474), received between Apr 27, 2022 and Apr 27, 2022 — classified as 1 injury.

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.

• InjuryApr 27, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED, APPROXIMATELY EIGHTEEN DAYS POST INITIAL LEFT THA, THIS FEMALE PATIENT WAS BROUGHT BACK FOR LEFT HIP TRAUMA, LESSER TROCHANTERIC FRACTURE, THE HIP WAS DISLOCATED, FEMORAL HEAD REMOVED AND STEM REMOVED. THE FRACTURE WAS REDUCED USING CABLE SYSTEM, A SIZE 6 HPS STEM WAS CEMENTED WITH A 36+3.5 BIOLOX HEAD. THERE WAS NO BREAKAGE OF DEVICE OR SURGICAL DELAY/PROLONGATION. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. X-RAY RECEIVED. THE DEVICES WILL BE RETURN.

  Patient problems: Bone Fracture(s)

  MAUDE report 14220189 ↗