The Maquet SERVO-i ventilator battery module has been recalled due to the battery having a shorter run time than expected, according to the American Society of Anesthesiologists. The FDA assigned a ...

GALWAY, Ireland--(BUSINESS WIRE)--Swedish based Maquet Critical Care and Aerogen, Ireland, have today announced the release of their partnered product, an integrated unit which provides state of the ...

Interstate Batteries announced a partnership today with Maquet Medical Systems USA (now Getinge Group) to provide original equipment manufacturer (OEM) batteries to the health care industry through ...

The Maquet Getinge Group is recalling 90,000 defective batteries used with the SERVO-i ventilator system, the US Food and Drug Administration (FDA) announced May 7. The FDA said some battery modules ...

Interstate Batteries announced a partnership today with Maquet Medical Systems USA (now Getinge Group) to provide original equipment manufacturer (OEM) batteries to the health care industry through ...

Troubled Maquet's woes continue. On the heels of a permanent injunction from the Department of Justice that resulted in the halt of manufacturing at one of its facilities, the suspension of 5 of its ...

The FDA has issued a Class 1 recall for Maquet’s C20, C30 and C40 FLOW-i Anesthesia Systems due to a software error, the company announced this week. There was a defect in the product’s Man/Auto ...

In a study published last September in clinical medical journal Critical Care, Maquet’s SERVO-U ventilator outperformed other ventilators in seven out of nine comparisons on use safety, perceived ...

WAYNE, N.J., July 31, 2012 /PRNewswire/ -- MAQUET Medical Systems USA today announced the commercial launch of TEGRIS, its new OR Integration system, in the United States. TEGRIS allows for seamless ...

WAYNE, N.J., July 31, 2012 /PRNewswire/ -- MAQUET Medical Systems USA today announced the commercial launch of TEGRIS, its new OR Integration system, in the United States. TEGRIS allows for seamless ...