Exactech 170-36-07Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862155498), received between Jun 14, 2022 and Jun 14, 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.

• InjuryJun 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED, APPROXIMATELY TWENTY TWO DAYS AFTER INITIAL THA, THE FEMALE PATIENT WAS BROUGHT BACK FOR A LESSER TROCHANTERIC FRACTURE. THE HEAD WAS REMOVED, THE STEM REMOVED. THE FRACTURE WAS REDUCED AND CABLES. A SIZE 10 HPS STEM WAS CEMENTED ALONG WITH A NEW 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 DEVICE IS NOT AVAILABLE FOR EVALUATION.

  Patient problems: Bone Fracture(s)

  MAUDE report 14684390 ↗