Skip to content

Legend Acetabular Shell 170-0446Recalls & reported problems

Ortho Development Corporation · No Hole, 46 mm · Class 2 · Implant

Data updated Oct 13, 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 00822409035267), received between Jul 17, 2023 and Jul 17, 2023 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Arthralgia1

Recent adverse event reports

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

  • InjuryJul 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    DURING HIP ARTHROPLASTY, THE ACETABULUM WAS PERFORATED DURING CUP IMPACTION. BONE WAS GRAFTED INTO THE PERFORATED AREA AND THE SURGERY WAS COMPLETED WITHOUT ANY PROBLEMS. STRONG BONE FRAGILITY WAS NOTED AS A FACTOR BY THE SURGEON.

    Patient problems: Arthralgia

    MAUDE report 17337912 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page