Respironics Recall Notice
Philips is continuing to ship replacement PAP devices for those who have registered their recall devices. We were notified that the BiPAP replacement devices have started to ship. Please refer to the 10/13/2021 update below for information on returning your recalled device. Thank you
Good news, progress is being made! We were notified today that Philips Respironics has started to ship replacement devices to individuals that received a recalled device from Corner Home Medical. When your replacement unit is ready to ship, Philips will call to notify you, then send an email the day it ships from their warehouse. It is very important that you follow all instructions in the box once you receive the unit. There will be an 800 number to call to assist in the set-up of the device and instructions on how to send the affected device back free of charge. Failure to send the affected device back to Philips may result in a charge to you that will not be covered by insurance. If you need further assistance with your new device, you may call us and schedule an appointment with one of our PAP technicians. Walk ins may experience significant delays or you may be asked to schedule an appointment for a future date. Philips is not able to tell us who is upcoming on the list, and it may be several months before your turn is up so, please be patient.
9/22/2021 UPDATE from Philips/Respironics
Manufacturing ramp up
“As you know, we have redirected our manufacturing capacity to focus on addressing the needs of the recall on a global scale. This includes increasing our production of new DreamStation2 devices. As a result, we have increased the global production capacity of repair kits and replacement devices in Q3 2021 to 55,000 units per week. We aim to increase capacity to 80,000 units per week in Q4 2021. This accelerated production schedule includes the high volume of support needed for the recall of the devices, impacted by the recall.”
9/1/2021 UPDATE Philips received authorization from the US Food and Drug Administration (FDA) for the rework of the affected first-generation DreamStation ONE, which consists of replacement of the PE-PUR sound abatement foam with a new material. More than 80% of the registered affected devices in the US to date are in the first-generation DreamStation product family. The company intends to complete the repair and replacement programs within approximately 12 months.
8/17/2021 UPDATE, Philips is still waiting for FDA’s approval for the new sound abatement foam. Philips has tripled their production power of this new foam and is waiting for a green light from the FDA. We don’t have any information on which machines will be replaced and which ones will be repaired.
UPDATE 8/13/2021 Philips has start shipping replacement CPAP machines. You will be notified by Philips when your replacement machine will be processed for shipment to you.
UPDATE 8/12/2021 PHILIPS does NOT recommend using a bacteria filter outside of their normal use.
After 8 weeks we have finally received additional information regarding the Philips/Respironics CPAP and BiPAP recall. Philips is planning to start shipping their first wave of replacement CPAP devices within the next 7 business days. We have not yet been notified as to who will be receiving them or how long it will take to mitigate all the affected devices. However, if you are one of the individuals who will be receiving a device in the first wave of replacement units, you will be notified directly by Philips and given additional information on how to complete the process. Philips will have multiple waves of replacements that will happen over time and in each case you will be contacted directly by Philips with instructions on what to do.
Corner Home Medical (CHM) will be providing weekly updates on this site, providing the most current information available. There are several factors that have prolonged this recall process and are creating difficulties for everyone involved. First, there is currently a global shortage of CPAP devices. Prior to the recall being announced, all manufacturers started experiencing issues acquiring key components to produce new devices. This resulted in all providers being put on an allocation status. Meaning that no company can order more devices than their historical purchase history. Second, the FDA has yet to approve the mitigation plan to repair or refurbish current Philips devices affected by the recall. The Durable Medical Equipment community (suppliers like CHM), physicians, device manufacturers, and Insurance companies have been communicating extensively, working together to take care of as many individuals as possible. Please visit this site weekly as this is where we will be posting any updates and new information. Thank you for your patience and continued support.
Jesse Neumann, Corner Home Medical President