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Medical Device Network on MSNFDA tags Medtronic’s voluntary ventilator recall as Class I after patient deathRelating to certain of Medtronic’s Newport ventilator range, users have been advised to remove the affected units from ...
Medtronic issued a voluntary recall notification to global customers related to specific Newport™ HT70 and HT70 Plus ventilators and certain related Newport™ service parts. The FDA recently designated ...
Drager expressing his excitement about the launch in India. The Atlan A100 system delivers advanced ventilation technology for adults, pediatric patients, and neonates, revolutionizing care with ...
Feb. 11, 2025 /PRNewswire/ -- Dräger, an international leader in medical and safety technologies, today announced that its Evita V800/V600 and Babylog VN800 family of mechanical ventilators ...
The FDA designated the recall of Draeger Medical’s Carina Sub-Acute Care Ventilator in pediatric patients as class I. The ventilators can still be used in adult patients as long as certain ...
Telford, PA, Aug. 01, 2023 (GLOBE NEWSWIRE) -- Draegerwerk AG & Co. KGaA initiated a voluntary recall notification for Draeger Carina Sub-Acute Care Ventilators to address possible contamination ...
Draeger Inc., of Telford, Pa., reported a recall of several lines of positive airway pressure (PAP) and other ventilation products in connection with problems seen in the adhesive used on breathing ...
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