PHILIPS RESPIRONICS - URGENT: MEDICAL DEVICE RECALL
This Recall covers all such devices manufactured before 26 April 2021
CPAP and Bi-Level PAP Devices; as well as Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent, BiPAP V30, and BiPAP A30/A40 Series Device Models
Sound Abatement Foam Susceptibility to Degradation and Volatile Organic Compound Emission
For more information go to: www.philips.com/src-update
or call the recall hotline @ 1-877-907-7508
Of course, contact your treating physician !
Abbey
Hi Abbey, and thanks so much for providing this important information.
You may be aware we had published similar information about the Philips recall information right here on our COPD.net website.
First, this alert, published on June 22, 2021: https://copd.net/news/phillips-recall.
And next, this material, published on August 9, 2021: https://copd.net/news/philips-ventilator-recall.
It's always good to keep one another informed of this type of material for everyone's safety.
We appreciate you jumping in with this, too!
Leon (site moderator COPD.net)
