Baxter Issues Urgent Medical Device Correction for LIFE2000 Ventilation System Due to Potential for Patient Desaturation When Connected with an Oxygen Concentrator
By DeECO |
Original Post Summary Company Announcement Date: March 10, 2023 FDA Publish Date: March 10, 2023 Product Type: Medical Devices Reason ...
Read More FDA Calls for Enhanced Safety Measures in Letter to Powdered Infant Formula Industry
By DeECO |
Original Post Constituent Update March 8, 2023 Today, the U.S. Food and Drug Administration sent a letter to manufacturers, packers, distributors, exporters, ...
Read More Update: Potential Risk of Exposure to Toxic Compounds When Using Hemodialysis and Peritoneal Dialysis Systems – Letter to Health Care Providers
By DeECO |
Original Post March 7, 2023 The U.S. Food and Drug Administration (FDA) is continuing to evaluate the potential risk of ...
Read More Pharmedica USA LLC Issues Voluntary Worldwide Recall of Purely Soothing 15% MSM Drops Due to Non-Sterility
By DeECO |
Original Post Summary Company Announcement Date: March 03, 2023 FDA Publish Date: March 03, 2023 Product Type: Drugs Reason for ...
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