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.
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Tandem Diabetes Care, Inc. provided an update on the t:connect app due to an issue causing rapid depletion of the tX2 insulin pump battery.
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RTLS helps health systems manage operational and financial challenges by improving device visibility and optimizing capital planning, according to one industry expert.
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Philips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
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The U.S. FDA and Health Canada are raising awareness about the safe use of Mega 2000 and Mega Soft Patient Return Electrodes by Megadyne Medical Products, Inc. due to reported burn injuries. Four voluntary recalls have been initiated since June 2023.
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