Spacelabs Monitor Recall Continues
In the FDA Enforcement Report for the week of November 28, it lists the ongoing recall of the Qube compact monitor (patient monitor) 91390.
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The FDA Class I Recall of the HeartSine Samaritan Public Access Defibrillator
Initiated 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 DS USA Continues its Anesthesia Delivery System Recall
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 MoreRecall Continues for Radiation Oncology Treatment Application
The 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 MoreOngoing Image Review Station Recall
The FDA Enforcement Report for the week of October 31 lists the ongoing Class II recall of GE Seno Advantage medical image review stations.
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