RELATED: FDA warns that Maquet's anesthesia system could lead to a fatal stop in ventilation
Maquet iabp webinar software#
Additionally, the company is developing a battery maintenance software upgrade, similar to releases for the CS300, CS100 and CS100i rolled out in 2017. “Although the FDA remains concerned about the device shutdown events associated with Maquet/Datascope IABPs, we recognize that these systems may be the best option for circulatory support for some patients,” the agency said in its notice.Īs part of the Class I recall in June and July, Maquet and Datascope have been contacting customers to schedule training visits regarding updated battery instructions, use, care and maintenance, the FDA said. Its efficacy in different clinical conditions is discussed on the appropriate topic reviews. Ventilation / Servo-I, Servo-S, SERVO-U/n and Compressor Mini / Service Training Seminars is a Advanced Webinar formated class focusing. Step 4: Complete the two programs under Intra-Aortic Balloon Pump Therapy eLearnings. Step 3: Under All Courses in the top menu bar, select ELearning Modules from the drop-down menu. The basic principles regarding use of the IABP are presented here. Step 1: Go to the Getinge Educational Academy website ( Step 2: Create an online account (no charge) if you do not already have one. The FDA said that “although the deaths cannot be definitively attributed to the device shutting down, these devices are used on critically-ill patients in health care facilities, including during transport, and any interruption in treatment can result in serious patient harm or death.” Intraaortic balloon pump counterpulsation (IABP) is one type of mechanical hemodynamic support, and it has emerged as the single most widely used circulatory assist device. Aortic Balloon Pump (IABP) For Interruption and/or Inability to Start. Since that letter, the agency said it has received over 60 additional reports, including two deaths and one serious patient injury. Getinge Issues Worldwide Voluntary Correction of Maquet/Getinge Cardiosave Intra.
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RELATED: FDA deems all 4,000+ of troubled Maquet's left atrial appendage closure devices potentially deadly, announces major recall Maquet-Getinge Group MAQUET Cardiovascular is a Division of Maquet-Getinge Group and provides a full range of cardiac perfusion products such as heart-lung machines, oxygenators, and Cardiohelp the new assist device platform. In a previous letter to healthcare providers from November 2018, the FDA described reports of these IABPs shutting down while running on battery power, leading to a loss of hemodynamic support.
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