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Results for tag: "Medical Device Recall"

US FDA Medical Device Recalls: Trend and Impact Analysis - Product Thumbnail Image

US FDA Medical Device Recalls: Trend and Impact Analysis

  • Report
  • December 2023
  • 45 Pages
  • United States
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Endoscopy Devices and Equipment Global Market Report 2024 - Product Thumbnail Image

Endoscopy Devices and Equipment Global Market Report 2024

  • Report
  • February 2024
  • 250 Pages
  • Global
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Medical Device Testing Global Market Report 2024 - Product Thumbnail Image

Medical Device Testing Global Market Report 2024

  • Report
  • January 2024
  • 200 Pages
  • Global
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Medical Device Design Control Essentials Course (Recorded) - Product Thumbnail Image

Medical Device Design Control Essentials Course (Recorded)

  • Training
  • October 2023
  • 2 Days
  • Global
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  • 14 Results (Page 1 of 1)
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The Medical Device Recall market is a subset of the Medical Devices industry, which encompasses a wide range of products used in the diagnosis, prevention, and treatment of medical conditions. Medical Device Recalls are initiated when a device is found to be defective or potentially hazardous to the patient. The recall process involves the manufacturer notifying the public of the issue, and then providing instructions on how to return the device for repair or replacement. The Medical Device Recall market is highly regulated, with the US Food and Drug Administration (FDA) overseeing the process. The FDA also provides guidance to manufacturers on how to properly recall a device, and how to ensure patient safety. Some of the major players in the Medical Device Recall market include Johnson & Johnson, Medtronic, Stryker, and Zimmer Biomet. Show Less Read more