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FDA Safety Information on Drugs & Medical Devices

May 8, 2017Newsgaladmin

Insufflation Unit Recall: Olympus Removes High Flow Insufflation Units
Source: FDA MedWatch Safety Alert Published on 2026-02-23 By FDA
Early Alert: Trividia Health Issues Correction for TRUE METRIX Blood Glucose Monitoring Systems
Source: FDA MedWatch Safety Alert Published on 2026-02-17 By FDA
Hormone Replacement Therapies Can Help Women with Bothersome Menopausal Symptoms
Source: FDA Consumer Health Information Updates Published on 2026-02-13 By FDA
Electronic Homecare Bed Correction: Medline Updates Use Instructions for Homecare Beds
Source: FDA MedWatch Safety Alert Published on 2026-02-13 By FDA
Emergency Response Safety Kit Recall: Airlife Removes Certain Broselow Pediatric Emergency Rainbow Tapes and Broselow ALS Organizers
Source: FDA MedWatch Safety Alert Published on 2026-02-11 By FDA
Trividia Health, Inc. Initiates Labeling Correction for all TRUE METRIX® Blood Glucose Monitoring Systems
Source: FDA MedWatch Safety Alert Published on 2026-02-06 By FDA
Detachable Coil System Recall: J&J MedTech/CERENOVUS Inc. Remove CEREPAK Detachable Coil System
Source: FDA MedWatch Safety Alert Published on 2026-02-05 By FDA
Glucose Monitor Sensor Recall: Abbott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors
Source: FDA MedWatch Safety Alert Published on 2026-02-05 By FDA
Glucose Monitor Sensor Recall: Abott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors
Source: FDA MedWatch Safety Alert Published on 2026-02-04 By FDA
Early Alert: Heart Pump Issue from Abiomed
Source: FDA MedWatch Safety Alert Published on 2026-02-03 By FDA
Early Alert: Insufflation Unit Issue from Olympus
Source: FDA MedWatch Safety Alert Published on 2026-01-22 By FDA
Early Alert: Wound and Burn Dressing Issue from Integra LifeSciences
Source: FDA MedWatch Safety Alert Published on 2026-01-22 By FDA
Early Alert: Broselow Rainbow Tape Issue from AirLife
Source: FDA MedWatch Safety Alert Published on 2026-01-16 By FDA
Anesthesia Kit Recall: Medline Removes Anesthesia Circuits and Anesthesia Circuit Kits
Source: FDA MedWatch Safety Alert Published on 2026-01-16 By FDA
Anesthetic Vaporizer Recall: Draeger Removes Vapor 2000 and Vapor 3000 Vaporizers
Source: FDA MedWatch Safety Alert Published on 2026-01-16 By FDA

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