Dec 7, 2012 | Government Regulations, Recalls | 0 |
The FDA announces that it is part of the first public-private partnership to promote medical device regulatory science with a focus on speeding the development, assessment, and review of new medical devices.
Read MoreIn the FDA Enforcement Report for the week of November 28, it lists the ongoing recall of the Qube compact monitor (patient monitor) 91390.
Read MoreInitiated September 13, 2012, the Class I Recall involves the HeartSine Samaritan 300/300P public access defibrillator (PAD), manufactured and distributed from August 1, 2004 to January 31, 2011.
Read MoreMindray Medical International Ltd, a developer, manufacturer, and marketer of medical devices worldwide, continues its August 8, 2012 voluntary recall affecting the A3/A5 anesthesia delivery system.
Read MoreThe FDA Enforcement Report for the Week of November 7 lists the ongoing Class II recall of the ARIA radiation oncology product from Varian Medical Systems, Palo Alto, Calif.
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