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 ...

For the fourth time this year, German devicemaker Dräger’s portfolio of respiratory devices is the target of a recall deemed Class I by the FDA. This time around, the agency has homed in on the ...

Telford, Pa., July 16, 2020 (GLOBE NEWSWIRE) -- Because mechanical ventilation is critical in the care of COVID-19 patients, Draeger leveraged its Intensive Care On-line Network (ICON) emergency ...

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 ...

German medical device manufacturer Dräger has voluntarily recalled the optional PS500 Power Supply Unit used with the Evita V500 and Babylog VN500 ventilators following complaints that the battery ...

Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of Draeger Medical’s Carina Sub-Acute Care Ventilator in pediatric patients as ...

The FDA warned customers Aug. 23 that 703 Draeger hospital ventilators pose a risk of contaminants in the airpath and emissions of a potential carcinogen. During testing, Draeger Medical found ...

With Carina ®,Dräger has developed an innovative,high performance NIV ventilator that is comfortable for both the patient and the caregiver. This compact, mobile unit optimizes workflow and workspace ...

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 ...

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’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 ...