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PROPHECY INBONE PTA00050Recalls & reported problems

Wright Medical Technology, Inc. · Toe Plate Attachment · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889797051996), received between Jun 27, 2023 and Jun 27, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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 16, 2026.

Most reported problems

Device problems

  • Mechanical Jam1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • 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 17212575 ↗

Other Trousers, anti-shock devices

All Trousers, anti-shock devices →

Sources and updates

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