Mindray 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.
Read MoreThe FDA Enforcement Report for the week of October 31 lists the ongoing Class II recall of GE Seno Advantage medical image review stations.
Read MoreNov 2, 2012 | Imaging Equipment | 0 |
I have a GE logiq 9 where in a couple of cases we are unable to send to our PACS system. The last menu you use to send the cases to PACS indicates there is a case and that there are images associated with that case. You can...
Read MoreIn 2007, Congress passed the Food and Drug Administration Amendments Act of 2007, which mandated the FDA to create a unique device identification (UDI) system to track and identify medical devices across the medical device life cycle—basical
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