Certain Philips Respironics BiPAP Machines Recalled Due to a Plastic Issue: FDA Safety Communication
By DeECO |
Original Post Date Issued: August 29, 2022 The U.S. Food and Drug Administration (FDA) is alerting patients, caregivers, and health ...
Read More Hospira Issues A Voluntary Nationwide Recall For One Lot of Propofol Injectable Emulsion (Containing Benzyl Alcohol), Due To The Potential Presence of Visible Particulates
By DeECO |
Original Post Summary Company Announcement Date: August 22, 2022 FDA Publish Date: August 22, 2022 Product Type: Drugs Reason for ...
Read More Safety Alert Regarding Use of Fecal Microbiota for Transplantation and Additional Safety Protections Pertaining to Monkeypox Virus
By DeECO |
Original Post August 22, 2022 Since May 2022, an outbreak of monkeypox disease has been ongoing in multiple countries, including ...
Read More FDA Approves First Cell-Based Gene Therapy to Treat Adult and Pediatric Patients with Beta-thalassemia Who Require Regular Blood Transfusions
By DeECO |
Original Post For Immediate Release: August 17, 2022 Today, the U.S. Food and Drug Administration approved Zynteglo (betibeglogene autotemcel), the ...
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