FDA reports 168 deaths associated with recalled Philips respiratory products
On August 17, 2022, the U.S. Food and Drug Administration (FDA) released a summary update of Medical Device Reports (MDRs) submitted in association with the Philips PE-PUR foam breakdown and associated Philips device recalls. The FDA indicates receipt of over 69,000 MDRs since April 2021, including 168 reports of death associated … [Read more...]