Defibtech Recalls Chest Compression Devices for Malfunction
Defibtech is recalling its RMU-2000 ARM XR Chest Compression Devices due to a motor issue that may cause the device to stop compressions, leading to potential patient injury or death.
Defibtech is recalling its RMU-2000 ARM XR Chest Compression Devices due to a motor issue that may cause the device to stop compressions, leading to potential patient injury or death.
High-risk patients who need defibrillators to prevent cardiac arrest experience fewer complications with a device implanted under the skin.
Several top chain restaurants in America do not have a policy of installing an automated external defibrillator at their businesses.
Defibtech is recalling its RMU-2000 ARM XR Chest Compression Devices due to a motor issue that may cause the device to stop compressions, leading to potential patient injury or death.
Royal Philips has launched a wireless remote monitoring and defibrillator solution (Tempus ALS) for pre-hospital settings in the United States.
Read MorePhilips has resumed the manufacturing and shipping of external defibrillators for the United States, following FDA notification that the injunction prohibiting those activities has been lifted.
Read MoreThe defibrillators market is forecast to reach $10.88 billion by 2022 from $9.32 billion in 2017 at a compound annual growth rate (CAGR) of 3.1%, according to market research firm ReportsnReports.
Read MoreBC Group, a company that manufactures, services, and sells biomedical testing equipment, has announced that its DA-2006-VL variable load box, an external load bank for the BC Biomedical line of defibrillator analyzers, has received FDA 510(k) clearance.
Read More