Resources and Guidance on COVID-19

CMS COVID-19 Resources

    FDA Recall: Revaclear Capillary Dialyzer 300, product code 114745L

    Product Description:

    Revaclear Capillary Dialyzer 300, REF Revaclear 300 Product Code 114745L

    Reason for Recall:

    Cybersecurity Updates Affecting Medtronic Implantable Cardiac Device Programmers: FDA Safety Communication

    The U.S. Food and Drug Administration (FDA) is informing patients, health care providers and facility staff, and manufacturers about cybersecurity vulnerabilities that may introduce risks for certain medical devices and hospital networks.

    Sandoz Inc. Issues Voluntary Recall of Ranitidine Hydrochloride Capsules

    September 23, 2019

    Apotex Corp. Issues Voluntary Nationwide Recall of Ranitidine Tablets 75mg and 150mg

    September 25, 2019

    Fresenius recalls dialysis tubes due to dangerous, undetectable leaks

    September 3, 2019

    Fresenius Kabi Recalls Volumat MC Agilia Infusion Pump and Vigilant Agilia Drug Library

    August 12, 2019

    President Donald J. Trump Is Taking a Bold New Approach to Advance Kidney Health

    July 10, 2019

    President Donald J. Trump signed an executive order aimed at improving kidney health and promoting increased treatment options for American patients.

    FDA MedWatch: Recall Baxter REVACLEAR 300 Dialyzer and Baxter REVACLEAR 400 Dialyzer

    July 8, 2019

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