2024 Maquet cardiosave recall

Maquet cardiosave recall

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August undefined, 2024

Getinge/Datascope/Maquet is recalling these products due to complaints of fluid leaks. Fluid entering the Cardiosave IABP may cause unexpected pump shutdown or the inability to initiate therapy. There has been one death and 71 complaints reported about this device issue. See more The CardioSave Hybrid/Rescue Intra-Aortic Balloon Pumps (IABP) are cardiac (heart) assist devices used with patients undergoing cardiac and non-cardiac surgery, and to treat adult patients who have acute coronary … See more On November 15, 2024, Getinge/Datascope/Maquet sent an Urgent Medical Device Correction Letter to customers instructing them to: 1. Immediately examine … See more WebDec 16, 2024 · FDA Announces Recall of Getinge/Maquet/Datascope Cardiosave Hybrid and Rescue IABPs December 16, 2024—FDA advised that the Getinge Group has recalled the Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs; …

Datascope/Getinge/Maquet Recalls Cardiosave …

WebWeb getinge group maquet cardiosave iabp quick reference manual (41 pages) iab insertion, iabp operation. Cardiosave hybrid retains the familiar look of datascope pumps, while offering an improved user interface and improved algorithms and pneumatics to allow for enhanced. ... Recall Datascope/Getinge Cardiosave Hybrid, Cardiosave Rescue, … WebDevice Recall Maquet Model / Serial HLS Set Advanced: Small Adult 5.0 with BIOLINE Coating BEQ-HLS 5050, 70105.2797, Adult 7.0 with BIOLINE Coating BEQ-HLS 7050, 70105.2794 and Adult 7.0 with SOFTLINE Coating BO-HLS 7050, 70105.2786 ... publishing date of a christmas carol

Getinge/Datascope/Maquet Recalls Cardiosave Hybrid …

WebDec 16, 2024 · Recalled Product Product Names: Datascope/Getinge/Maquet Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Model Numbers: See Recall Database Entry Manufacturing... WebDec 22, 2024 · (UPDATED) The Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) have been placed under recall by the manufacturer (Getinge/Datascope/Maquet) following reports of fluid leaks, the US Food and Drug … sea slavery

Getinge/Datascope/Maquet Recalls Cardiosave Hybrid and Cardiosave ...

WebDec 17, 2024 · So far, 4,338 devices have been recalled in the U.S., with one death and 71 complaints related to the device issue, which the FDA confirmed is fluid leaks. Fluid entering the Cardiosave IABP may cause unexpected pump shutdown or the inability to initiate therapy, the regulatory body said. WebJul 24, 2024 · Getinge is recalling numerous Maquet/Datascope intra-aortic balloon pumps (IABPs) due to potential battery failure during use that can lead to unexpected stopping and shortened run times. Maquet/Datascope has received reports of five patient deaths … publishing date of moby dickWebDec 23, 2016 · Class 2 Device Recall Cardiosave. Maquet has received 3 confirmed complaints related to the Li-lon Battery used with the Maquet CARDIOSAVE Hybrid IABP and Maquet CARDIOSAVE Rescue IABP of the battery venting after being accidentally dropped. Maquet contacted their customers via letter on 12/23/16 and additional … publishing date of the time machine

"WebCARDIOSAVE Hybrid IABP and Maquet CARDIOSAVE Rescue IABP. Model / Serial PART NUMBER: 0146-00-0097 DISTRIBUTION DATE: All Li-Ion Batteries Distributed from December 12, 2011 to November 9, 2016 ... Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their … " - Maquet cardiosave recall

Maquet cardiosave recall

Device Recall Maquet - International Consortium of Investigative ...

WebJun 11, 2024 · On June 6, Maquet Datascope Corp. issued a Class I recall for the CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), a cardiac assist device used for patients undergoing cardiac and non-cardiac surgery and patients with acute coronary syndrome or complications from heart failure, due to a design issue that allows fluid … WebDatascope Cs100 Service Manual iforex indicators com. Getinge s Maquet Datascope recall select IABPs over. China Bionet Cardiocare 2000 EKG Cable 10lead 15pins. Hospital Furniture Manufacturing Companies Hospital. Public tenders for Medical equipment in United States. Datascope MAQUET Intra Aortic Balloon Pump Recall ? Daily.

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WebOct 29, 2024 · Reason for Recall Datascope/Getinge/Maquet is recalling this product due to the risk of the battery failing and having a shortened run-time due to substandard batteries not meeting performance... WebJul 11, 2024 · Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794. Code Information. Lot 70131093; UDI 04037691741543. Recalling Firm/. Manufacturer. Maquet Cardiovascular Us Sales, …

WebJul 24, 2024 · Medical device models being affected include Cardiosave Hybrid IABP, Cardiosave Rescue IABP, CS300 IABP, and CS100/100i IABP. A total of 22,853 devices are covered by the recall. CS300 Intra-Aortic Balloon Pump. Source: Maquet/Datascope WebMaquet CARDIOSAVE ® Hybrid Intra ... You may have previously received the Maquet Urgent Product Recall notification, dated December 2015, regarding a potential issue relating to the scroll compressor of your CARDIOSAVE Hybrid and/or CARDIOSAVE Rescue IntraAortic Balloon Pumps (IABPs), which will be collectively referred to in this …

WebMaquet Cardiovascular Us Sales, Llc QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO 11000-USA#QUADROX-i Neo.+Res... 1 11/28/2024 Maquet Cardiovascular Us Sales, Llc Cardiosave Hybrid IABP, Part Number 0998-00-0800-53: 1 10/27/2024 Maquet Datascope Corp - Cardiac Assist Division WebSep 27, 2024 · The FDA announced that Getinge issued a voluntary recall of two intra-aortic balloon pumps due to interruption or inability to start therapy at high altitudes.The recall involves 5,223 Maquet ...

WebMAQUET CARDIOSAVE hybrid and MAQUET CARDIOSAVE rescue Product Code/Part Number: 0998-XX-0800-XX Distributed Affected Lot Number: All Distribution Dates: Since March 6, 2012 ... This voluntary recall only affects the products listed on page 1; no other products are affected

WebOct 29, 2024 · Datascope/Getinge/Maquet is recalling 137 substandard battery packs for the CardioSave Hybrid/Rescue Intra-Aortic Balloon Pump, which may cause the cardiac assist device to stop working when operated by battery only. Customers should examine their … sea slayerWebDec 21, 2015 · U kunt hier een specifiek type publicatie kiezen, zoals brochures of jaarverslagen. publishing date of harry potterWebDec 22, 2024 · (UPDATED) The Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) have been placed under recall by the manufacturer (Getinge/Datascope/Maquet) following reports of fluid leaks, the US Food and Drug Administration announced last Thursday. The agency deemed the action a Class I … publishing date of peter panWebOct 29, 2024 · Recalled Product. Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs. Product Codes and Lot Numbers: See Recall Database Entry. Devices Recalled in the United States: 137 battery ... publishing date of through the looking glassWebDec 16, 2024 · Recalled Product Product Names: Datascope/Getinge/Maquet Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Model Numbers: See Recall Database Entry Manufacturing... publishing dates for booksWebJun 7, 2024 · The US Food and Drug Administration (FDA) has alerted users of Datascope Corp/MAQUET’s Cardiosave hybrid intra-aortic balloon pump (IABP) to a “design issue” that enables fluids to leak into the device, classifying a recent field corrective action by the company as a Class I recall. “The fluid can cause corrosion of internal components ... seas learningWebOct 29, 2024 · FDA announces serious device recall Oct 29, 2024 - 03:06 PM The Food and Drug Administration today announced a Class 1 recall of battery packs for an intra-aortic balloon pump used with patients undergoing surgery and to treat adults with acute coronary syndrome or heart failure complications. publishing date the metamorphosis