Chair(s): Dirk A.A. Pevernagie, Anita Simonds
Session type: Round table
Piet-Heijn van Mechelen
Session content
Winfried J. Randerath
Replay
Jan Kimpen
Replay
Patient testimonial
Piet-heijn Van Mechelen
Replay
Jean-louis Pepin
Replay
Replay
Session aims
The Philips Respironics recall of ventilators and positive airway pressure machines started in 2021. This action was imposed by the FDA following reports that the PE-PUR sound insulation foam in these devices may decompose, thereby causing a risk of exposure to debris and chemicals for the patients. Meanwhile, the recall has been broadened to a global scale and replacements are still ongoing. This adverse situation has caused major concerns in patients, practitioners, providers, and regulators, among others. The aim of this session is to reflect on the history of this incident, on the implications for safety rules and guidelines, and on preventive measures for the future. The opinions of parties involved will be presented during this session.