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April 10, 2026Open Access

Analysis of Trends in FDA-Recalled Hip Arthroplasty Devices: A Retrospective Review.

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Authors

LLLucas P A LorimerKHKalter HaliJRJonathan Raspanti

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Overview

Retrospective review analyzes safety trends in hip arthroplasty devices, indicating areas for improvement.

Key Points

  • The aim is to analyze trends in the recall of hip arthroplasty devices by the FDA.
  • Conducted a retrospective review of FDA-recalled hip arthroplasty devices.
  • Analyzed recall data over a specific time period to identify trends.
  • Evaluated the reasons for device recalls.
  • Identified a significant increase in recalls over the past few years.
  • Outlined common reasons for recalls, including device failures and safety concerns.
  • Highlighted the need for improved safety measures in hip arthroplasty device manufacturing.

Cite This Study

Lorimer et al. (2026) studied this question.

synapsesocial.com/papers/69d8955f6c1944d70ce06579https://doi.org/10.2106/jbjs.oa.26.00062
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Powered Versus Manual Acetabular Component Extraction in Revision Total Hip Arthroplasty: A Comprehensive Analysis of 98 Cases.2026
  2. 2The Epidemiology of Revision Total Knee Arthroplasty in the United States2009 · 1,248 citations
  3. 330-Day Readmission Following Inpatient Total Shoulder Arthroplasty in Pennsylvania: A Statewide Analysis.2026
  4. 4Assessing the Completeness of Safety Reporting in Clinical Trials of Total Knee Arthroplasty: A Registry-Publication Comparison Study.2026
  5. 5Early Conversion Total Hip Arthroplasty for High-Energy Acetabular Fractures Is Associated With Poor Outcomes.2026