FDA issues warning on Getinge device amid quality concerns
Following a series of voluntary recalls, the FDA has urged healthcare providers to avoid Getinge’s intra-aortic balloon pumps over safety concerns.
09 May 2024
09 May 2024
Following a series of voluntary recalls, the FDA has urged healthcare providers to avoid Getinge’s intra-aortic balloon pumps over safety concerns.
The device has received the designation for treating mitral regurgitation and mitral annular calcification.
The report published by the Medicines Discovery Catapult warns that a mix of economic uncertainty and lack of facility access is pushing investors away from Britain’s healthcare SMEs.
The latest version features new modules, including the CARTO ELEVATE Module and CARTOSOUND FAM Module.
The collaboration aims to develop a first-of-its-kind digital PCR assay capable of detecting and quantifying minimal amounts of DNA with high accuracy.
The new technology combines RPM technologies with advanced arrhythmia detection algorithms.
Intended for over-the-counter use, the 3-in-1 test is intended for detecting Covid-19 and influenzas A and B.
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