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NOTICE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
#21
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
(01-30-2024, 02:29 PM)btreger Wrote: I just answered your question on the Recall Thread

All of our documentation is to the contrary to date. They have indicated replacements, not a dead end street.
Please post your source, documentation, etc. We'd be interested in pursuing your information with Philips.
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#22
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
I hope they do not permit export of tools or eqipment. With Philips track record they will just ship it out to some other country and bang them out there with even less control to sell their machines to the rest of the world where the they think that they may get away with it.
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#23
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
The DreamStation Go end of sale and shipping were 1/25/2024, while end of service is 1/25/2029. Most other items similarly ended. Alice testing, all the way up to POC oxygen, ventilators, so on.

This will be identical info to the first chart listing what seems like every item we may use.

There's a chart within homecaremag at this website:

Homecaremag
INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEBSITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
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#24
GLOBAL MEDIA SITES RESPONDING TO PHILIPS NEWS
As one might expect, news traveled quickly around the world in all markets that are served by Philips Respironics.  Although the Philips CEO, in a recent quarterly results interview, confidentially stated that Philips will continue to actively sell the DreamStation 2 in all other countries that it serves, local country media outlets will likely generate calls by Philips CPAP users to their local country health agencies.  I don't think that Philips will be able to easily contain the new restrictions placed upon it to just the U.S.

Although the news of Philips' discontinued and halted-sale products is based on the same Philips press release, media outlets are adding in additional back-story and other details to create some attention-getting headlines, such as:

Quote:"Philips to halt sales of sleep apnea machines amid fears they can cause CANCER"
Machines can spew carcinogenic foam through oxygen tube to the user's mouth
30 January 2024  |  Daily Mail (UK)
https://www.dailymail.co.uk/health/artic...ancer.html

It will still likely take several weeks/months for most CPAP users, in the U.S. and elsewhere, to learn of the discontinued and halted-sale products.  I hope that ResMed and other well-established reputable producers will increase their productions and consider new products to replace Philips' discontinuing products, if they don't already exist.
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#25
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
I think I have replied to several of our Canadian members, that truckloads of unsaleable, discounted Philips CPAP are probably on the way to Provincial health systems for distribution to our Canadian friends that do not get a choice from their socialist medical system. It will actually be an upgrade they can get Philips Dreamstation 2 Auto CPAPs and BiPAPs instead of basic fixed CPAP. The may even get the unobtainum ASV (auto SV) and AVAPS that Canada won't otherwise provide.
Sleeprider
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INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED AS MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEB SITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
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#26
Sad 
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
The U.K. Daily Mail is reporting...
Quote:Sheriff, 62, from Louisiana claims sleep apnea mask he used for four years gave him KIDNEY CANCER - as FDA reveals nearly 600 deaths linked to Philips' CPAP devices

FDA reported there have been 561 deaths since 2021 linked to Philips machines
There were 111 reports of deaths linked to machines in just three months last year

A 62-year-old Louisiana man battled kidney cancer he believes was caused by his sleep apnea breathing machine manufactured by health tech giant Philips. 

Sheriff Brett Stassi had been using his Philips DreamStation CPAP mask every night for four years to treat his sleep apnea and would often found tiny black particles on his pillow left behind by the machine.

It wasn't until a recall of the devices in June 2021 that he learned those particles were far from harmless.

He said: ‘You’re worried about dying in your sleep, and you come to find out that the machine might be doing more damage than the apnea.’

One month before the recall, Mr Stassi was rushed into emergency surgery after a routine doctor visit found he had kidney cancer. He had to undergo surgery to remove his right kidney, according to ProPublica.

While the sheriff is now in remission, nearly 600 people who used the now-recalled CPAP machines have died in the last three years of illnesses linked to foam and potentially toxic gases that blow into users’ airways while they wear the device.

Philips has pulled millions of faulty sleep apnea ventilators from the market amid an ever-growing mountain of cases in which long-time users have been diagnosed with cancers, pneumonia, asthma, and other severe health problems.

Sheriff Brett Stassi, 62, used the Philips DreamStation for four years before being rushed into emergency surgery when his doctor discovered he had kidney cancer. It was only after the recall that he learned the black specks from his CPAP could harm his kidneys and liver

Sheriff Stassi is one of hundreds of people suing Philips whose ventilators contained foam that emitted carcinogenic gases including formaldehyde, benzene, methylene chloride

Philips to halt sales of sleep apnea machines fears they cause CANCER

Now, the Food and Drug Administration has reported that since initiating a recall of approximately 15 million devices in 2021, 561 CPAP users have died as a result of illnesses linked to faulty machines while thousands are battling other severe health conditions. 

Which Philips devices have been recalled? 

Philips recalled the following devices made between 2009 and April 26, 2021: 

A-Series BiPAP A30
A-Series BiPAP A40 (ventilator)
A-Series BiPAP Hybrid A30
A-Series BiPAP V30 Auto (ventilator)
C-Series ASV (ventilator)
C-Series S/T and AVAPS
DreamStation
DreamStation ASV
DreamStation Go
DreamStation ST, AVAPS
Dorma 400
Dorma 500
E30
Garbin Plus, Aeris, LifeVent (ventilator)
OmniLab Advanced+
REMstar SE Auto
SystemOne ASV4
SystemOne (Q-Series)
Trilogy 100 (ventilator)
Trilogy 200 (ventilator)

The deaths were recorded in 116,000 medical device reports, the FDA’s database for reporting adverse effects. There were 111 deaths recorded from July to September of 2023 alone, out of a total of more than 7,000 medical device reports filed in that narrow period.

Millions of people suffer from sleep apnea, a condition characterized by pauses in breathing or shallow breaths during sleep which, over time, vastly increases one’s risk of heart attack and stroke. 

An estimated eight million Americans rely on a CPAP machine to sleep through the night, and given Philips' status as a leader in the CPAP devices market, a large share of those eight million devices are likely included in the recall. 

The problem stems from the type of foam used in the headgear of the machine that is affixed around the head and connected to a snorkel-like device. It’s meant to dampen sound and vibrations as the machine operates.

But the foam, made with polyester-based polyurethane, has been shown to degrade and break off into tiny particles and release harmful chemical gases such as formaldehyde, benzene, methylene chloride, volatile organic compounds, and solvents – all of which have been linked to different types of cancers and respiratory problems.

The device is used to treat sleep apnea by delivering continuous pressurized air through a person's airway via a face mask connected to tubing. 

The airflow's pressure is precisely high enough to keep the airway from collapsing when the muscles at the back of the throat relax, resulting in continuous sleep without abrupt waking and choking.  

St Louis native and father of four Terry Flynn lost his battle with esophageal cancer in 2021 just two weeks after receiving the diagnosis, according to reporting from ProPublica.

The 63-year-old had used a recalled Philips device for nine years, and while his family will never know if the faulty device was the exact cause of his illness, they faulted the company for failing to warn about health risks sooner.

Meanwhile, 58-year-old retired music teacher and father of three Mark Edwards has experienced years of recurring respiratory infections and benign tumors which he believes were caused by the Philips DreamStation ventilator.

He told PBS News: ‘I noticed when I was first using my new machine what we saw like black specks, white specks, it just went from like pure, distilled water to look and like water you would see in like a polluted creek.

‘The walls on my lungs are shot now. So they'll never work again. I can't get a lung transplant because nobody will be wanting to transplant your lung into an infected area where it's just going to go bad.’

Also in New York, a man named Lawrence Braverman sued Philips over claims that its machine, which he had been using since 2011, had caused repeated bouts of mouth cancer starting in 2015. 

Parts of his mouth and tongue had to be biopsied and surgically removed, and he was forced to use a feeding tube.

Terry Flynn of St Louis, Missouri died of esophageal cancer in 2021 just two weeks after being diagnosed. His family will never know for certain that the Philips machine lead to his deadly cancer, but they fault the company with failing to warn customers sooner

Mark Edwards, pictured left, is a retired music teacher and father of three who used the Philips DreamStation ventilator from 2017 to 2021. He has suffered several bouts of severe respiratory infections and two benign throat tumors

The foam near the mouthpieces of the machines has been linked to more than just throat and oral cancers.

In Johnson County, Kansas, 70-year-old Robert Dix was diagnosed with lung cancer in late 2019. He had been using the Philips Respironics DreamStation Auto CPAP device since 2016.

One in five Americans has a potentially fatal sleep disorder 

Sleep apnea is a common sleep-related condition where breathing stops and restarts through the night, putting the body at risk of dangerously depriving it of vital oxygen. 

According to his lawsuit against the company, he faces permanent disability and ‘now requires constant and continuous medical monitoring and treatment due to the defective nature of the subject device and/or defendants’ wrongful conduct.’

These lawsuits, like roughly 700 others, are ongoing.  

The FDA announced a deal this week that it struck with Philips, what’s formally known as a consent decree, which stipulated that the company would halt all sales of its sleep apnea masks in the US. 

In addition to recalling CPAP, or Continuous Positive Airway Pressure, machines, the company is recalling several similar BiPAP, or Bilevel Positive Airway Pressure, machines.

At the same time, it will have to take massive steps to correct problems with the devices, an undertaking that Philips executives estimate will cost roughly $393 million.

The company’s efforts to fix the defective devices starting in 2021 have been a long process and have frustrated users who need the devices to sleep. As the recalls expanded beyond the original for five million devices, the repair-or-replace efforts have bled into 2024.

Recent reporting from ProPublica revealed that Philips knew its products’ foam was faulty and potentially dangerous well before it became public knowledge.

Philips withheld more than 3,700 complaints about the machines, including 370 reports of deaths, from the FDA for 11 years before the recall.

Philips had seen examples of the foam breaking down in its ventilators in Japan and had conducted tests in the US that showed the black specks released gaseous chemicals. Still, the company did not warn the public.

The company did not initiate a formal inquiry into the issue until 2019, which was nine years after the initial wave of complaints and three years after the company's first known tests revealed the degradation of the foam.

Last September, Philips agreed to pay $479 million to settle a CPAP class-action suit to anyone who purchased, leased, or rented one of the recalled devices. 

Philips is facing roughly 750 other lawsuits, meaning punitive damages levied against the company will likely number into the tens of millions of dollars.
"The object in life is not to be on the side of the majority, but to escape finding oneself in the ranks of the insane." -- Marcus Aurelius
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#27
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
Philips Direct Site https://www.usa.philips.com/healthcare/e...lio-update

Quote:Philips Respironics
"Sleep & Respiratory Product Portfolio Changes"
Information for US customers only
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#28
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
If I'm reading this correctly, Dreamstations other than the DS Go are NOT discontinued anday still be sold.
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#29
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
Gideon, it's unclear. Philips will no longer sell the items, but it appears that inventory at DMEs and in other channels will likely continue to be sold. I don't see a recall or offer to buy-back this already sold inventory.
Sleeprider
Apnea Board Moderator
www.ApneaBoard.com

____________________________________________
Download OSCAR Software
Soft Cervical Collar
Optimizing Therapy
Organize your OSCAR Charts
Attaching Files
Mask Primer
How To Deal With Equipment Supplier


INFORMATION ON APNEA BOARD FORUMS OR ON APNEABOARD.COM SHOULD NOT BE CONSIDERED AS MEDICAL ADVICE. ALWAYS SEEK THE ADVICE OF A PHYSICIAN BEFORE SEEKING TREATMENT FOR MEDICAL CONDITIONS, INCLUDING SLEEP APNEA. INFORMATION POSTED ON THE APNEA BOARD WEB SITE AND FORUMS ARE PERSONAL OPINION ONLY AND NOT NECESSARILY A STATEMENT OF FACT.
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#30
RE: Philips Discontinues Numerous Devices and Halts Dreamstation Sales in the U.S.
I read as the DS Go was permanently being phased out and Philips will not sell it as of 25 January 2024.  That may well mean that existing stock can be sold

BUT

No mention of any other DreamStation was made, a fact I missed in my initial read.  Thus I ASSUME that these will still be sold by Philips.
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