[Equipment] PHILIPS RECALL FOCUS GROUP - Printable Version +- Apnea Board Forum - CPAP | Sleep Apnea (https://www.apneaboard.com/forums) +-- Forum: Public Area (https://www.apneaboard.com/forums/Forum-Public-Area) +--- Forum: Main Apnea Board Forum (https://www.apneaboard.com/forums/Forum-Main-Apnea-Board-Forum) +--- Thread: [Equipment] PHILIPS RECALL FOCUS GROUP (/Thread-Equipment-PHILIPS-RECALL-FOCUS-GROUP) |
PHILIPS RECALL FOCUS GROUP - WakeUpTime - 11-22-2021 This may already exist in other site forums. I thought it may be beneficial to start a separate thread on actions that impacted Philips Recall device users could take as a collective group. Philips is well prepared to ignore the requests from individual users, however if that same request were to be repeated by 30, 50 or 100 recalled device owners, that might carry a little more weight. The same may hold true for letters sent to medical and consumer protection agencies, government offices, law firms, sleep associations, insurance companies, etc., regarding Philips' specific actions and policies related to the Recall. Template e-mail letters could be constructed by one person, with the individual group members repeating the same e-mails - only of course if they fully support the letter. If the document were already prepared, along with e-mail (or telephone) contact details to make it very easy, we might be able to tilt the direction of some of Philips' policies. The collective group, if not all Philips Recall device users, would therefore benefit by the efforts of one individual, saving a substantial amount of time and potentially generating some greater results. It's important to note that this proposed new thread would only be for responding to Philips, and not to detract from the discussions in the main Philips Recall thread, or related Recall threads (foam replacement, DS2 encryption, etc.). RE: PHILIPS RECALL FOCUS GROUP - btreger - 12-02-2021 DRAFT DRAFT DRAFT DRAFT To whom it may concern, My name is xxxxxxxx and I am a Sleep Apnea patient. I am a user of one of the recalled products. I was notified via email on June 14 of Philips Involuntary Recall and registered my product. I am also a member of The Apnea Board Forum. This is a Medical Crisis, millions of sleep apnea patients in the US have been left to fend for themselves while trying to survive and protect their health. You may not know all of the detailed health effects of this recall, so I have attached a document with all the relevant information. We desperately need news media like yours and your association with other news outlets to stand up and sound the alarm, and to contact Philips and the FDA to make sure they understand you are very concerned for the health of millions of American citizens. Contacting The US Consumer Product Safety Commission could help to highlight this ongoing health crisis. Critical Care Doctors need to be made aware of all the potential symptoms related to the recalled CPAP products. Some of our concerns: -Recalled device users know that they likely won't receive a "fixed" device (or replacement) for many months, possibly years -Philips has instructed users to stop using their recalled devices and acquire a replacement device -A timely immediate appropriate replacement or compensation for the need to immediately replace a medically necessary breathing system -CPAP systems are not health aids, they are life extensions -Telling CPAP users that they must immediately stop using their machine means they have to immediately acquire something else - or, worse yet, be forced to continue using their defective, potentially cancer-causing, breathing system -Out-of-Pocket financial costs, for purchasing new equipment, and to cover current and future health problems related to the use of defective devices -Corporate neglect in delaying the announcement of the recall -Design errors in the implementation of the foam in 2009 It is very apparent to users like me, that this industry has no enforceable standards or oversight. There is no third party that can verify and certify the safety of these life-saving products. Unless changes are made, problems like this will keep happening and human life will be at risk. Respectfully yours xxxxxxxxxxxxx Some e-mails that could be used; denise.roland@wsj.com Wall Street Journal dbaquet@nytimes.com New York Times walter.snesko@fda.hhs.gov FDA info@cts-sct.ca Canadian Thoracic Society info@tga.gov.au Australian Government / Therapeutic Goods Administration evening@cbsnews.com 60 Minutes sally.buzbee@washpost.com Washington Post Gerald.Harmon@ama-assn.org AMA RE: PHILIPS RECALL FOCUS GROUP - btreger - 12-03-2021 DRAFT DRAFT DRAFT Apnea Board Summary Philips Recall http://www.apneaboard.com/wiki/index.php/Philips_Respironics_Recall_2021 RE: PHILIPS RECALL FOCUS GROUP - WakeUpTime - 12-04-2021 (12-02-2021, 12:18 PM)btreger Wrote: DRAFT Excellent letter. I'll look forward to utilizing much of that text with several additional parties. Many thanks. I'd like to also make a letter to address the Philips CEO's comments about not needing to address perceived "shelved" Philips Recalled devices. I'll post when I can pull the right text together. A RECALLED DEVICE OWNER'S PLEA - WakeUpTime - 01-02-2022 Here's another example of Recalled device owners reaching out to demand a better response from Philips: Philips must take responsibility for recall of CPAP machine for sleep apnea https://www.lehighvalleylive.com/opinion/2021/11/philips-must-take-responsibility-for-recall-of-cpap-machine-for-sleep-apnea-letter.html Quote:By Express-Times Letters to the Editor RE: PHILIPS RECALL FOCUS GROUP - LindanHotAir - 01-02-2022 I don’t understand how Philips can ignore “shelved” machines. Their recall notice initially told patients to stop using their machines. Now if they did so, the machines are “shelved”? Was that intended to reduce the problem for Philips? Can you spell Catch 22? |