FDAnews
www.fdanews.com/articles/130328-westmed-recalls-manual-resuscitation-device

Westmed Recalls Manual Resuscitation Device

September 16, 2010
Westmed, a producer of anesthesia and respiratory devices, is initiating a Class I recall of its BagEasy Manual Resuscitation device after discovering separation problems in the unit’s retention ring. A disconnection would make the device inoperable and could result in treatment delays. Westmed became aware of the problem after it received reports from three separate facilities.