The supply of the circuit boards needed to fix the devices is significantly constrained, preventing the company from ...
The FDA issued an early alert warning customers of potential issues with certain Resmed (NYSE:RMD) ventilator systems.
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Autonomous Healthcare today announced that the U.S. Food and Drug Administration (FDA) has granted the De Novo marketing authorization for Syncron-E™, its software that supports respiratory therapists ...
Though Philips recently expanded its ongoing respiratory device recall to include around 5.2 million machines, that list left off a handful of ventilators that weren’t affected by the original issue.
MANHASSET, N.Y., June 08, 2026--(BUSINESS WIRE)--A critically ill patient at Northwell's North Shore University Hospital (NSUH) has been one of the first in the United States – and the first on the ...
On Tuesday, Koninklijke Philips N.V. (NYSE:PHG) issued a correction related to the Software Version used in Trilogy Evo, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal ventilators to resolve ...
(RTTNews) - Baxter International Inc. has issued an urgent medical device recall for Life2000 ventilators citing potential damage to the attached battery charger dongle. The recall was initiated after ...
BROOKLYN, N.Y.--(BUSINESS WIRE)--Solutions in Critical Care (SCC) has partnered with Nanotronics Health, LLC, to distribute nHale™, a non-invasive respiratory support device authorized for the ...
Philips has recalled some sleep apnea and ventilator machines over concerns about health risks. The company on Monday issued a recall for specific Philips Bi-Level Positive Airway Pressure (Bi-Level ...
The Dutch medical equipment firm Koninklijke Philips NV RYLPF has recalled several of its sleep apnea and respiratory care devices due to potential health risks. What Happened: The company stated that ...
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