Jul 22, 2022 · In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only). We know the profound impact this recall has had on our patients, our business customers, and ...
Register affected devices on the recall notification (U.S. only) / field safety notice (International Markets) website, www.philips.com/SRC-update. The website provides current information on the status of the recall notification (U.S. only) / field safety notice (International Markets) and how to receive permanent corrective action to address the two issues.
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Register affected devices on the recall notification (U.S. only) / field safety notice (International Markets), www.philips.com/SRC-update. The website provides current information on the status of the recall notification (U.S. only) / field safety notice (International Markets) and how to receive permanent corrective action to address the two issues.
1. To register your product, you’ll need to log in to your My Philips account. Don’t have one? You can create one here. 2. Register your product and start enjoying benefits right away. You can also upload your proof of purchase should you need it for any future service or repairs needs.
Product Registration. Thank you for choosing Philips! With just a few mouse clicks, you can register your new product today. You may also gain access to the lastest savings, promotions, and product news, simply by choosing to receive future correspondence from Philips.
Garbin Plus, Aeris, LifeVent. Continuous Ventilator, Minimum Ventilatory Support, Facility Use. A-Series BiPAP Hybrid A30 (not marketed in US) A-Series BiPAP V30 Auto. Continuous Ventilator, Non-life Supporting. A-Series BiPAP A40 (not marketed in the US) A-Series BiPAP A30 (not marketed in the US) For patients (5)
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