FDA MedWatch Use the Correct Cycle and Compatible N95 Respirators

May 30, 2020

Use the Correct Cycle and Compatible N95 Respirators When Decontaminating Respirators with STERRAD Sterilization Systems - Letter to Health Care Providers

Important Information on the Use of Serological (Antibody) Tests for COVID-19 - Letter to Health Care Providers

April 22, 2020

Important Information on the Use of Serological (Antibody) Tests for COVID-19 - Letter to Health Care Providers

All Ranitidine Products (Zantac): Press Release - FDA Requests Removal

ISSUE:  The FDA announced it is requesting manufacturers to withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. 

FDA MedWatch: BodyGuard Infusion Pump System by CME America - Class I Recall

April 1, 2020

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

 

Recalled Product

CDC Health Alert Network- Severe Illness Associated with Using Non-Pharmaceutical Chloroquine Phosphate to Prevent and Treat COVID-19

March 30, 2020

Distributed via the CDC Health Alert Network
CDCHAN-00431

 

CMS ESRD Provider Telehealth and Telemedicine Tool Kit

Centers for Medicare & Medicaid Services (CMS) released two comprehensive toolkits on telehealth that are specific to general practitioners as well as providers treating patients with End-Stage Renal Disease (ESRD).

CDC Releases New Resources on the Supply of PPE and Home Isolation

Today, the Centers for Disease Control and Prevention (CDC) released new information on two critical areas of care related to Coronavirus Disease-2019 (COVID-19).

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:

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