U.S. FDA asks Philips Respironics to notify patients about ventilator recall – Reuters.com

U.S. FDA asks Philips Respironics to alert individuals regarding ventilator recall – Reuters.com

The U.S. Food as well as Drug Administration (FDA) asked Dutch clinical devices manufacturer Philips Respironics on Thursday to inform clients regarding the firm’s recall of specific ventilators as well as various other breathing aid devices in June last year.Read More …