Philips Issues Correction for Trilogy Evo Ventilators Following FDA Class I Recall
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
The new location aims to shorten delivery times and support hospitals across Oklahoma and neighboring states with on-demand medical equipment.
Baxter is replacing faulty battery chargers in the Life2000 Ventilator system after identifying a defect that triggers alarms and renders the device inoperable.
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
Baxter is recalling the Life2000 Ventilator System due to potential battery charging dongle failure, which can prevent or hinder charging.
Read MoreHamilton Medical issued a software correction for the Hamilton-C6 ventilator due to a failure to restart ventilation in sensor fail mode.
Read MoreThree major manufacturers—Philips Respironics, Baxter Healthcare, and Zoll Medical—have issued Class I recalls for their ventilators due to critical issues posing a risk of serious injury or death.
Read MoreSmiths Medical is recalling its paraPAC Plus 300 and 310 Ventilator Kits due to a malfunction where the device may not cycle properly.
Read MoreA consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
Read MoreVyaire Medical is recalling certain AirLife Manual Resuscitators due to a life-threatening manufacturing defect.
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Medtronic announced that it would exit the ventilator market that it characterized as increasingly unprofitable.