According to Philips company guidelines, if you are using an affected CPAP or Bi-Level Pap device, you should “discontinue use of your device and work with your physician or Durable Medical Equipment(DME) provider to determine the most appropriate options for continued treatment.”
If you are using an affected Life-Sustaining Ventilator Device, “do not stop or alter your prescribed therapy until you have talked to your physician.”
Boesen Law is investigating this matter. If you or someone you know has been affected by the recall of a Philips B-Level PAP, CPAP, or has been treated using a Philips mechanical ventilator, please contact us at 303-999-9999.
For more information regarding the recall and for Philips’ contact information, click here.
For a complete list of affected ventilator devices, click here.
For a complete list of affected Bi-Level PAP and CPAP machines, click here.