Medical Device Recall: Interruptions and/or loss of therapy due to Ventilation Inoperative Alarm

In March 2023 Philips Respironics issued a medical device recall regarding interruptions and/or loss of therapy in the Philips Respironics OmniLab Advanced Plus (OLA+), V30 Auto, BiPAP A30, and BiPAP A40. The affected products feature a Ventilator Inoperative alarm, which occurs when the ventilator detects an internal error or a condition that could result in interruption and/or loss of therapy.

Providing patients with safe and high-quality therapy devices is our primary focus. We encourage you to read the Interruptions and/or loss of therapy due to Ventilation Inoperative Alarm Medical Device Recall below to learn more about the circumstances under which this issue can occur and the mitigating actions you can take to ensure safe continued use.