Characterization of US Food and Drug Administration Class I Recalls from 2018 to 2022 for Moderate- and High-Risk Medical Devices: A Cross-Sectional Study

Author:

Mooghali MaryamORCID,Ross Joseph SORCID,Kadakia Kushal T,Dhruva Sanket S

Publisher

Informa UK Limited

Subject

Biomedical Engineering,Medicine (miscellaneous)

Reference30 articles.

1. U.S. Food and Drug Administration. Regulatory controls. Available from: https://www.fda.gov/medical-devices/overview-device-regulation/regulatory-controls. Accessed March 15, 2023.

2. U.S. Food and Drug Administration. Premarket notification 510(k). Available from: https://www.fda.gov/medical-devices/premarket-submissions-selecting-and-preparing-correct-submission/premarket-notification-510k. Accessed March 15, 2023.

3. Characteristics of Clinical Studies Conducted Over the Total Product Life Cycle of High-Risk Therapeutic Medical Devices Receiving FDA Premarket Approval in 2010 and 2011

4. Strength of Study Evidence Examined by the FDA in Premarket Approval of Cardiovascular Devices

5. U.S. Food and Drug Administration. MDR data files. Available from: https://www.fda.gov/medical-devices/medical-device-reporting-mdr-how-report-medical-device-problems/mdr-data-files. Accessed March 15, 2023.

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