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.
Read MoreThe 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.
Read MoreFeb 7, 2013 | Management | 0 |
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 MoreThe 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 MoreIn 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.
Read MoreStryker Medical Division of Stryker Corp continues its Class II Recall of its medical surgical bed, model numbers 3002S3EX and 3005S3EX.
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