FDA Gets Over 48,000 Reports of Faulty Philips Respiratory Devices in May-July FDA Gets Over 48,000 Reports of Faulty Philips Respiratory Devices in May-July

FDA said it had received more than 48,000 reports of faulty Dutch medical equipment maker Philips ' ventilators and respiratory devices between May and July, which included 44 deaths.Reuters Health Information
Source: Medscape Critical Care Headlines - Category: Intensive Care Tags: Pulmonary Medicine News Source Type: news