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Case 2:21mc01230JFC Document 491 Filed 03/29/22-Page 1 of 23UNITED STATES DISTRICT COURT WESTERN DISTRICT OF PENNSYLVANIA IN RE: PHILIPS RECALLED CPAP, LEVEL PAP, AND MECHANICAL VENTILATOR PRODUCTS

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How to fill out philips recalled cpap bi-level

01

Check the model and serial number of your Philips recalled CPAP bi-level machine.

02

Contact Philips or your healthcare provider for instructions on obtaining a replacement or repair.

03

Follow the provided instructions to fill out any necessary forms or paperwork for the recall process.

04

Return your recalled CPAP bi-level machine as instructed by Philips or your healthcare provider.

05

Follow up with Philips or your healthcare provider for updates on the status of your replacement or repair.

Who needs philips recalled cpap bi-level?

01

Patients who have been using a Philips recalled CPAP bi-level machine.

02

Anyone who has been diagnosed with sleep apnea and uses a CPAP bi-level machine.

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What is philips recalled cpap bi-level?

The Philips recalled CPAP bi-level refers to certain models of Bi-Level PAP and CPAP devices manufactured by Philips that were recalled due to potential health risks.

Who is required to file philips recalled cpap bi-level?

Patients who have been using the affected Philips recalled CPAP bi-level devices are required to take action and file for a replacement or repair.

How to fill out philips recalled cpap bi-level?

To fill out the Philips recalled CPAP bi-level form, patients need to provide their personal information, device details, and any health issues experienced due to the device.

What is the purpose of philips recalled cpap bi-level?

The purpose of the Philips recalled CPAP bi-level is to ensure the safety and well-being of patients using the affected devices by providing them with a solution to the recall.

What information must be reported on philips recalled cpap bi-level?

Patients need to report their personal information, device details, any health issues experienced, and whether they are seeking a replacement or repair for the affected CPAP bi-level device.

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