Each year, the FDA receives several hundred thousand medical device reports of suspected device-associated deaths, serious injuries and malfunctions. Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products. To learn more about how to report an adverse event, please visit the FDA website for updated information.
You May Also Like
Importing Medical Devices During the COVID-19 Pandemic
Dawa MedicalJuly 15, 2021
Quidel Recalls Lyra SARS-CoV-2 Assay
Dawa MedicalJuly 8, 2021
Medtronic Vascular Recalls Angiographic Guidewire Component
Dawa MedicalJuly 6, 2021