FDA Sends Notice of Class I Recall of Hamilton Ventilators
Hamilton Medical Inc, Reno, Nev, has recalled the HAMILTON-T1 ventilators with software versions 1.1.2 and lower. It initiated the recall on January 11, 2013.
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Mindray Continues its Vital Signs Monitor Recall
The Class II Recall of 13 units, initiated in September of 2012, involves the Mindray DPM5 monitor, a vital signs monitor used on human patients in health care facilities.
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CCE Prep: Committee Management III
This article is a continuation of the previous article on Committee Management, which appeared in the “CCE Prep” column in the September 2012 issue.
Read MoreGE Seeks to Inspect Remaining Units from October Class I Recall
The FDA resent information regarding the October 15, 2012 voluntary field corrective action for the field upgrade kit for GE Healthcare’s resuscitation systems with blender, installed in GE Giraffe and Panda infant warmers.
Read MoreOngoing Recall of CT Workspace Portal
In the Enforcement Report for the week of January 23 the FDA lists the voluntary Class II Recall by Philips Medical Systems (Cleveland) Inc of the computed tomography x-ray system Brilliance workspace portal.
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