PROPHECY INBONE PTA00010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889797051934), received between Jun 27, 2023 and Sep 21, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Mechanical Jam” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 21, 2026Mechanical Jam

  It was reported that during an Inbone case, the C-Bracket (b)(6) was not functioning properly, as the side knob seems to be cross threaded and won't tighten or loosen.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50841195 ↗
• MalfunctionJun 27, 2023Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT SEPARATING BOTH COMPONENTS POST PROCEDURE TOOK EXCESSIVE FORCE WHICH POTENTIALLY DAMAGED COMPONENTS. THE INSTRUMENT ISSUE WAS DISCOVERED AFTER SURGERY. NO SURGICAL DELAY, NO ADDITIONAL PATIENT ADVERSE CONSEQUENCES. NO OTHER INSTRUMENTS/IMPLANTS WERE USED IN COMBINATION WITH THE AFFECTED INSTRUMENTS THAT MAY HAVE CONTRIBUTED TO THIS EVENT. THERE WAS NO ADVERSE EFFECT ON SURGICAL OUTCOME. THE PROCEDURE WAS COMPLETED SUCCESSFULLY

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17212862 ↗