Philips Respironics, Inc.: Medical Device Recalls in 2025

According to to data from the FDA, there were 7 medical device recalls made by Philips Respironics, Inc. in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

• DreamStation Auto CPAP. Non-Continuous Ventilator.
• BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.
• DreamStation Auto. Non-Continuous Ventilator.
• BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
• DreamStation Auto BiPAP. Non-Continuous Ventilator.
• BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
• SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600