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DJO SURGICAL 498-01-048Recalls & reported problems

Encore Medical, L.P. · Flared Rim Shell - Size 48 · Class 3 · 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 00888912087414), received between Dec 22, 2016 and Dec 22, 2016 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryDec 22, 2016Adverse Event Without Identified Device or Use Problem

    REVISION SURGERY - DUE TO THE PATIENT PRESENTING WITH PAIN. THE SURGEON FELT A LINER SWAP WOULD RELIEVE THAT.

    Patient problems: Pain

    MAUDE report 6200862 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

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Sources and updates

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