Telford, Pa., Jan. 07, 2021 (GLOBE NEWSWIRE) -- Dräger, an international leader in the fields of medical and safety technology, today announced that it has entered into an agreement with Breas Medical ...

Draeger asked hospitals to stop using several mechanical filters due to misleading carbon dioxide readings, according to a recall notice posted by the Food and Drug Administration on Tuesday. The ...

As ventilators and other respiratory devices became more crucial than ever throughout the COVID-19 pandemic, so too did any safety issues embedded in the machines become more apparent. Following in ...

Draeger’s correction of its Atlan A350 and A350 XL anesthesia workstations were recently deemed Class I by FDA. The correction pertains to the potential of the device to experience a mechanical ...

The Fabius MRI anesthesia machine features our precision E-Vent piston ventilator technology, renowned for both performance and safety. It has been tested for use with MRI systems of 1.5 and 3 Tesla ...

The FDA warned of a Covidien ventilator that may not deliver enough air, and another one from Dräger Medical that has faulty batteries. The ongoing corrective actions of about 2,700 units of the ...

TELFORD, Pa., 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 ...

Dräger has initiated a voluntary nationwide recall of the PS500 optional power supply unit used with the Evita V500 and Babylog VN500 ventilators because of a battery problem. The recall stems from ...

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 ...

Draeger initiated a nationwide recall of the optional PS500 Power Supply Unit used with the Evita V500 and Babylog VN500 ventilators. This voluntary action was a result of an internal investigation by ...

Today Draeger issued a statement regarding its voluntary recall on specific Fabius anesthesia machines. Draeger initiated this voluntary action in August of 2013 as a result of an internal ...