HIP PRESERVATION SYSTEM SIGNATURE SERIES HPS-HB02Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20845854029883), received between Jun 4, 2019 and Jun 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Melted” (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.

• MalfunctionJun 4, 2019Melted; Melted

  THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE, HPS-HB02, 4.5MM X 19CM HPS PREBENT POLISHING BUR APPEARED TO HAVE MELTED AT THE HUB AND METAL SHAVINGS WERE SEEN IN THE SURGICAL SITE ON (B)(6) 2019 DURING A HIP ARTHROSCOPY. THE METAL SHAVINGS WERE WASHED OUT. THERE IS NO REPORTED PATIENT INJURY OR IMPACT. THERE WAS A SLIGHT DELAY TO GET ANOTHER HAND PIECE. THE PROCEDURE WAS COMPLETED AS PLANNED. THIS REPORT IS BEING RAISED BASED ON DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8666639 ↗