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Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
    The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health...

2022 Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
    2021 Medical Device Recalls Subscribe to Medical Device Safety and Recalls Sign up to receive email updates on medical device recalls, safety communications, and other …

2023 Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls
    2023 Medical Device Recalls | FDA An official website of the United States government Here’s how you know U.S. Food and Drug Administration Search Menu …

U.S. FDA classifies recall of Philips' respiratory devices as most ...

    https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-classifies-recall-philips-respiratory-devices-most-serious-2023-02-16/
    2 days ago · The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' respiratory machines as most serious, …

GE HealthCare Recalls Nuclear Medicine Systems for …

    https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients
    GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients The FDA has identified this as a Class I recall, …

Recalls, Corrections and Removals (Devices) | FDA

    https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices
    You must contact your FDA’s Office of Regulatory Affairs (ORA) Division Recall Coordinator (DRC) listed here by state or region (look for Product Type “Medical Device”). Foreign …

Medical Device Recalls - Food and Drug Administration

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm
    This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or removal actions initiated …

2022 Medical Device Recalls | FDA - U.S. Food and …

    https://cacmap.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
    2022 Medical Device Recalls | FDA An official website of the United States government Here’s how you know U.S. Food and Drug Administration Search Menu Home Medical …

What is a Medical Device Recall? | FDA

    https://www.fda.gov/medical-devices/medical-device-recalls/what-medical-device-recall
    Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health. A medical device recall does not always mean …

Medical Device Recalls | FDA - U.S. Food and Drug …

    https://cacmap.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
    If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …



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