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

April 8, 2026Open Access

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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.

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

Level III. See Instructions for Authors for a complete description of levels of evidence.

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Lorimer et al. (2026) studied this question.

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