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Lineage 36430046Recalls & reported problems

Microport Orthopedics Inc. · LINEAGE® ACETABULAR SHELL 46MM QUAD HEMI FLARE STD GROUP 1 · Class 2 · Implant

All models of Lineage (35)

Data updated Oct 16, 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 M684364300461), received between Oct 1, 2019 and Oct 1, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Corroded” (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

  • Corroded1
  • Insufficient Device Problem Information1

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.

  • InjuryOct 1, 2019Corroded; Insufficient Device Problem Information; Corroded; Insufficient Device Problem Information

    (B)(6). PREVIOUSLY REPORTED PAIN IN R HIP INVESTIGATED VIA MRI, FOUND TO HAVE TWO LESIONS AT THE R HIP JOINT. (SEE ATTACHMENT).

    Patient problems: Pain

    MAUDE report 9142778 ↗

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

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Sources and updates

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