A51

HealthCare Alerts

ICS Advisory (ICSA-20-203-01) Wibu-Systems CodeMeter (Update B)
BD Announces FDA Classifications for August 4th Recalls of BD Alaris™ System Hardware for Keypads, Incorrect Module Types and/or Sizes, and Channel Error
ICS Medical Advisory (ICSMA-20-261-01) - Philips Clinical Collaboration Platform
Becton Dickinson (BD) CareFusion 303, Inc. Recalls Alaris™ System PC Unit and PC Unit Front Case Keypad Replacement Kits Due to Risk of Stuck or Unresponsive Keys
ICS Medical Advisory (ICSMA-20-254-01) Philips Patient Monitoring Devices
FDA alerts health care professionals and oncology clinical investigators about efficacy and potential safety concerns with atezolizumab in combination with paclitaxel for treatment of breast cancer
BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware
Alert (AA20-245A) Technical Approaches to Uncovering and Remediating Malicious Activity
Mylan Initiates Voluntary Nationwide Recall of Four Lots of Amiodarone HCl Injection, USP and Tranexamic Acid Injection, USP Due to Carton Label Mix-Up
BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware

Events

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