The FDA has notified doctors and hospitals of reports that some Philips Avalon Fetal Monitors are producting inaccurate readings, most often during the second stage of labor. Philips issued an Important Device Safety Alert on September 4, 2009. If the inaccurate readings are not recognized and addressed, doctors may be unaware of fetal distress or may recommend unnecessary interventions based on false information. In order to avoid serious injuries, doctors must recognize the conditions and respond appropriately. The affected models are the FM20, FM30, FM40 and FM50 with the ultrasound transducer.
The Legal Examiner and our Affiliate Network strive to be the place you look to for news, context, and more, wherever your life intersects with the law.
Comments for this article are closed.