FDA Upgrades LIFEPAK 15 Monitor/Defibrillator Recall to Class I FDA Upgrades LIFEPAK 15 Monitor/Defibrillator Recall to Class I

The company issued a voluntary recall of the devices earlier this month, but the FDA class I recall notes that the defect has resulted in serious patient injury, including death.News Alerts

Source: Medscape Medical News Headlines - February 28, 2019 Category: Consumer Health News Tags: Cardiology News Alert Source Type: news