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Do Not Resuscitate

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GE Healthcare, LLC, Giraffe and Panda T-Piece Resuscitation Systems and Mask Resuscitation Systems: Class 1 Recall - Potential r by FDA and air wall inlet fittings and/or labels on the back panel of the resuscitation systems..., including death. BACKGROUND:  The Giraffe and Panda T-Piece Resuscitation Systems and the Giraffe Panda Bag...
Class I Medical Device Recall: GE Healthcare, Giraffe Warmer with Resuscitation System, Panda Warmer with Resuscitation System, by FDA The oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed during assembly.
Cardiocerebral Resuscitation May ... by Dr. Rubens D. Medical Doctor Cardiocerebral Resuscitation May Improve Survival In cardiocerebral resuscitation after cardiac... resuscitation (CCR) -- an alternative approach to cardiopulmonary resuscitation (CPR) for patients with cardiac...
Hospital Resuscitation Hasn't Im ... by Dr. Rubens D. Medical Doctor Hospital Resuscitation Hasn't Improved Survival in Elderly Fewer than one in five patients... -- Among elderly patients who undergo in-hospital cardiopulmonary resuscitation, overall survival rates have not...
BagEasy Manual Resuscitation Devices by Westmed, Inc.: Class 1 Recall by FDA : Westmed, Inc. is initiating a nationwide recall of 24,384 units of BagEasy Manual Resuscitation Devices... of resuscitation. BACKGROUND: Westmed has become aware of a potential for disconnection at the patient port...
Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices by FDA , is initiating a nationwide recall of 24,384 units of BagEasy Manual Resuscitation Devices. The select lots... of resuscitation. This recall is classified by the FDA as a Class I Recall. Consumers who have units...
Resuscitation 2012 by Dr. Ivor K. Medical Doctor Tomorrow I will be travelling to Vienna, Austria to take part in the Resuscitation 2012 congress organised by the European Resuscitation Council. At this annual congress, which will take place...
When Can EMS Stop Resuscitation? by Thaddeus Pope Doctor of Philosophy Termination of Resuscitation in Cases of Refractory Out-of-Hospital Cardiac Arrest. They identify criteria... Few patients (0.1% of 5500 studied) who are resuscitated and brought to the hospital by EMS survive...
Ventlab Corporation Issues Nationwide Recall of its Manual Resuscitators by FDA - On July 11, 2012, Ventlab Corporation initiated a nationwide recall of 14,602 of its manual resuscitators. The manual resuscitators as listed below have been found to potentially deliver little to no air/oxygen...
Ventlab Adult and Pediatric Manual Resuscitators: Recall-Valve Leak Prevents Flow of Air/Oxygen to Patient by FDA resuscitators may have a valve leak which prevents the flow of air/oxygen to the patient. This lack of airflow.... The affected manual resuscitators were manufactured and distributed between March 2012 and July 2012...

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