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DJO SURGICAL 430-01-060Recalls & reported problems

Encore Medical, L.P. · SHELL, FMP HEMISPHERICAL SIZE60 W/HOLES · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912081887), received between Feb 25, 2016 and Feb 25, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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

Device problems

  • Device Slipped1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryFeb 25, 2016Device Slipped

    PRIMARY SURGERY - DUE TO THE 40MM 6.5 SCREW GOING THROUGH THE DJO FMP 3 HOLE CUP.

    Patient problems: No Information

    MAUDE report 5461056 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented devices

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Sources and updates

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