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{{Short description|Philips respiratory equipment division}}
{{more footnotes|date=December 2010}}
{{Infobox company
{{Infobox company
| name = Respironics
| name = Respironics
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| type = [[Subsidiary]]
| type = [[Subsidiary]]
| foundation = 1976
| foundation = 1976
| founder = [[Gerald McGinnis]]
| location = [[Murrysville, Pennsylvania]]
| location = [[Murrysville, Pennsylvania]]
| key_people = Don Spence, President and CEO
| key_people = Don Spence, President and CEO
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'''Respironics''' is an American medical supply company owned by Philips that specializes in products that improve [[Respiratory system|respiratory functions]]. It is based in the [[Pittsburgh]] suburb of [[Municipality of Murrysville, Pennsylvania|Murrysville]] in [[Pennsylvania]], United States.
'''Respironics''' is an American medical supply company owned by Philips that specializes in products that improve [[Respiratory system|respiratory functions]]. It is based in the [[Pittsburgh]] suburb of [[Municipality of Murrysville, Pennsylvania|Murrysville]] in [[Pennsylvania]], United States.

Some of its products had hazardous foam that disintegrated and entered patients' bodies. Company officials were aware of the defect, but continued to market them while the company withheld the vast majority of reports.<ref name=":0">{{Cite news |last=Cenziper |first=Debbie |last2=D. Sallah |first2=Michael |last3=Korsh |first3=Michael |last4=Robinson-Johnson |first4=Evan |last5=Sager |first5=Monica |date=September 27, 2023 |title=Philips Kept Complaints About Dangerous Breathing Machines Secret While Company Profits Soared |work=[[ProPublica]] |url=https://www.propublica.org/article/philips-kept-warnings-about-dangerous-cpaps-secret-profits-soared |access-date=October 14, 2023}}</ref>


==History==
==History==
In 1976, company founder Gerald McGinnis opened the company's first manufacturing facility for [[anesthesia]] masks near [[Pittsburgh, Pennsylvania]]. Previous product research and manufacturing had occurred in the founder's kitchen. Other early products included endotracheal and tracheostomy products.
In 1976, company founder [[Gerald E. McGinnis]] opened the company's first manufacturing facility for [[anesthesia]] masks near [[Pittsburgh, Pennsylvania]]. Previous product research and manufacturing had occurred in the founder's kitchen. Other early products included endotracheal and tracheostomy products.


McGinnis developed the "Nasal CPAP Mask System," a [[continuous positive airway pressure]] (CPAP) machine for the treatment of [[sleep apnea]],<ref>{{cite web |title=Philips kept complaints about dangerous breathing machines secret while company profits soared |url=https://newsinteractive.post-gazette.com/philips-respironics-cpap-defect-recall/ |website=Pittsburgh Post-Gazette Interactive |publisher=Pittsburgh Post-Gazette |access-date=2 February 2024 |date=27 September 2023}}</ref> based on the original 1981 design by [[Colin Sullivan (physician)|Dr. Colin Sullivan]].<ref>{{cite web |title=How the CPAP machine beats deadly sleep apnoea |url=https://www.sydney.edu.au/news-opinion/news/2018/03/16/how-the-cpap-machine-beats-deadly-sleep-apnoea.html |publisher=The University of Sydney |access-date=2 February 2024}}</ref> After receiving [[FDA]] approval in 1984, Respironics began selling the first commercially available CPAP machine a year later.<ref>{{cite news |title=Philips recall crisis casts shadow over legacy of Respironics founder |url=https://www.post-gazette.com/business/healthcare-business/2023/12/29/gerald-mcginnis-philips-respironics-legacy/stories/202312290012 |access-date=2 February 2024 |publisher=Pittsburgh Post-Gazette |date=30 December 2023}}</ref>
The company introduced the first [[continuous positive airway pressure]] (CPAP) machine for the treatment of [[sleep apnea]] in 1985. Three years later, in 1988, the company went public under the stock ticker symbol RESP. In 1992, Respironics received a patent for bi-level technology. This technology was originally intended as an improvement on CPAP, however, its use has expanded into the treatment of other breathing disorders such as [[chronic obstructive pulmonary disease]] (COPD).

In 1988, the company went public under the stock ticker symbol RESP. In 1992, Respironics received a patent for bi-level technology. This technology was originally intended as an improvement on CPAP, however, its use has expanded into the treatment of other breathing disorders such as [[chronic obstructive pulmonary disease]] (COPD).


Other significant milestones were the acquisition of the ventilator company LIFECARE International in 1996, [[sleep apnea]] competitor Healthdyne Technologies in 1998, and medical monitor and sensor leader Novametrix in 2002.
Other significant milestones were the acquisition of the ventilator company LIFECARE International in 1996, [[sleep apnea]] competitor Healthdyne Technologies in 1998, and medical monitor and sensor leader Novametrix in 2002.


On December 21, 2007, Respironics announced it entered into a merger agreement with [[Philips]],<ref>{{cite web|url=http://www.respironics.com/News/philips.asp|url-status=deviated|archive-url=https://web.archive.org/web/20080610195622/http://www.respironics.com/News/philips.asp|archive-date=10 June 2008|title=ROYAL PHILIPS ELECTRONICS TO ACQUIRE RESPIRONICS FOR USD $66.00 PER SHARE|website=Respironics}}</ref> with Philips acquiring all shares of Respironics for $66 per share, for a total of approx $5.1 billion. On March 14, 2008, Philips announced completion of tender offer to acquire Respironics.<ref>{{Cite press release |title=PHILIPS ANNOUNCES COMPLETION OF TENDER OFFER TO ACQUIRE RESPIRONICS (EX-99.A.2.I) |author= |website=www.sec.gov |date=14 March 2008 |url= https://www.sec.gov/Archives/edgar/data/313216/000095012308002956/y51433a9exv99waw2wi.htm}}</ref><ref>{{Cite news|url=https://www.reuters.com/article/us-philips-idUSL2131786820071221|title=Philips in $5 billion Respironics deal|author1=Foo Yun Chee|author2=Niclas Mika|date=2007-12-21|work=Reuters|language=en}}</ref>
On December 21, 2007, Respironics announced it entered into a merger agreement with [[Philips]],<ref>{{cite web|url=http://www.respironics.com/News/philips.asp|url-status=deviated|archive-url=https://web.archive.org/web/20080610195622/http://www.respironics.com/News/philips.asp|archive-date=10 June 2008|title=ROYAL PHILIPS ELECTRONICS TO ACQUIRE RESPIRONICS FOR USD $66.00 PER SHARE|website=Respironics}}</ref> with Philips acquiring all shares of Respironics for $66 per share, for a total of approx $5.1 billion. On March 14, 2008, Philips announced completion of tender offer to acquire Respironics.<ref>{{Cite press release |title=PHILIPS ANNOUNCES COMPLETION OF TENDER OFFER TO ACQUIRE RESPIRONICS (EX-99.A.2.I) |author= |website=www.sec.gov |date=14 March 2008 |url= https://www.sec.gov/Archives/edgar/data/313216/000095012308002956/y51433a9exv99waw2wi.htm}}</ref><ref>{{Cite news|url=https://www.reuters.com/article/us-philips-idUSL2131786820071221|title=Philips in $5 billion Respironics deal|author1=Foo Yun Chee|author2=Niclas Mika|date=2007-12-21|work=Reuters}}</ref>

== Hazardous foam and product recall==
A redesign of the [[CPAP]] devices{{Which|date=October 2023}} from Respironics led to over a decade of complaints to Philips, which withheld the vast majority of them from the U.S. [[Food and Drug Administration]] (FDA). Around 2010, the company added industrial foam made of [[polyester]]-based [[polyurethane]] to silence rattling in the machine. But the foam could fall apart in heat and [[humidity]], sending it into patients' noses, mouths, throats, and lungs. Among the chemicals released was [[formaldehyde]], a potential [[carcinogen]].<ref name=":0" />

Only in 2021 did Philips recall the machines, which had been delivered across the United States and many other countries. Over 3,700 complaints across more than 11 years were held back from the FDA, which device makers are required to do so within 30 days of reports of patient injuries in addition to investigating them. The company did not begin an internal investigation until 2019. The devices were used by children, the elderly, and over 700,000 U.S. veterans. As many as 15 million devices were affected. People experienced [[vomiting]], [[dizziness]], [[headaches]], and cancers in the [[Lung cancer|lungs]], [[Throat Cancer|throat]], [[Sinus cancer|sinuses]], and [[Esophageal cancer|esophagus]]. Company officials knew about the dangers of the device, but continued to market and sell them.<ref name=":0" />

During the [[COVID-19 pandemic]], the company ramped up production of another ventilator that also included the foam. Operating profits from the ventilators, including the CPAP devices, soared to around US$800 million. During the pandemic, Philips conducted a series of studies on the foam, showing the deteriorating foam and chemicals released by it, which could cause "serious injury, life-threatening or permanent impairment".<ref name=":0" />

The company said patients' health is its top priority, and regretted the "distress and concern" that the recall caused. It said complaints about the foam were limited and were evaluated on a case-by-case basis, and it was made aware of the significance in early 2021, launching the recall soon after. Months after the recall, Philips said that tests showed the chemicals released by the foam were within safe levels.<ref name=":0" />

The company announced a new CPAP machine in April 2021, and soon after admitted that the foam it had used previously had been breaking down in an earnings call. Then-CEO [[Frans van Houten]], in the earnings call, pledged 250 million euros to the problem, and reassured investors that the "device is safe to be continued to use to the best of our knowledge at this time". The company alerted the FDA but not customers. Following the recall, van Houten said he regretted the impact of it on "patients, care providers, and shareholders."<ref name=":0" />

Multiple federal lawsuits have been levied against the company. One settled with the company for US$479 million to reimburse customers.<ref>{{Cite news |last=Jewett |first=Christina |date=September 7, 2023 |title=CPAP Maker Reaches $479 Million Settlement on Breathing Device Defects |work=[[The New York Times]] |url=https://www.nytimes.com/2023/09/07/health/cpap-defect-recall-philips-respironics.html |access-date=November 28, 2023 |issn=0362-4331}}</ref><ref name=":0" />


==Today==
==Today==
Philips Respironics's products include devices for the diagnosis and treatment of [[sleep apnea]] including [[Continuous positive airway pressure|CPAP]] and bi-level ([[BiPAP]]) [[non-invasive ventilation]] machines, [[oxygen concentrator]]s for patients requiring supplemental [[oxygen]], infant [[apnea]] monitors for infants at risk of [[Sudden infant death syndrome|SIDS]], [[asthma]] treatment solutions and hospital [[ventilators]].
Philips Respironics's products include devices for the diagnosis and treatment of [[sleep apnea]] including [[Continuous positive airway pressure|CPAP]] and bi-level ([[BiPAP]]) [[non-invasive ventilation]] machines, [[oxygen concentrator]]s for patients requiring supplemental [[oxygen]], infant [[apnea]] monitors for infants at risk of [[SIDS]], [[asthma]] treatment solutions and hospital [[ventilators]].


==References==
==References==
<references />
{{Reflist}}
Need to update your complaint department.


==External links==
==External links==

Latest revision as of 01:08, 26 February 2024

Respironics
Company typeSubsidiary
IndustryMedical
Founded1976
FounderGerald McGinnis
HeadquartersMurrysville, Pennsylvania
Key people
Don Spence, President and CEO
Productsrespiratory equipment
sleep aids
RevenueIncrease $1.05 billion USD
Number of employees
4,900[1]
ParentPhilips
Websitewww.respironics.com

Respironics is an American medical supply company owned by Philips that specializes in products that improve respiratory functions. It is based in the Pittsburgh suburb of Murrysville in Pennsylvania, United States.

Some of its products had hazardous foam that disintegrated and entered patients' bodies. Company officials were aware of the defect, but continued to market them while the company withheld the vast majority of reports.[2]

History[edit]

In 1976, company founder Gerald E. McGinnis opened the company's first manufacturing facility for anesthesia masks near Pittsburgh, Pennsylvania. Previous product research and manufacturing had occurred in the founder's kitchen. Other early products included endotracheal and tracheostomy products.

McGinnis developed the "Nasal CPAP Mask System," a continuous positive airway pressure (CPAP) machine for the treatment of sleep apnea,[3] based on the original 1981 design by Dr. Colin Sullivan.[4] After receiving FDA approval in 1984, Respironics began selling the first commercially available CPAP machine a year later.[5]

In 1988, the company went public under the stock ticker symbol RESP. In 1992, Respironics received a patent for bi-level technology. This technology was originally intended as an improvement on CPAP, however, its use has expanded into the treatment of other breathing disorders such as chronic obstructive pulmonary disease (COPD).

Other significant milestones were the acquisition of the ventilator company LIFECARE International in 1996, sleep apnea competitor Healthdyne Technologies in 1998, and medical monitor and sensor leader Novametrix in 2002.

On December 21, 2007, Respironics announced it entered into a merger agreement with Philips,[6] with Philips acquiring all shares of Respironics for $66 per share, for a total of approx $5.1 billion. On March 14, 2008, Philips announced completion of tender offer to acquire Respironics.[7][8]

Hazardous foam and product recall[edit]

A redesign of the CPAP devices[which?] from Respironics led to over a decade of complaints to Philips, which withheld the vast majority of them from the U.S. Food and Drug Administration (FDA). Around 2010, the company added industrial foam made of polyester-based polyurethane to silence rattling in the machine. But the foam could fall apart in heat and humidity, sending it into patients' noses, mouths, throats, and lungs. Among the chemicals released was formaldehyde, a potential carcinogen.[2]

Only in 2021 did Philips recall the machines, which had been delivered across the United States and many other countries. Over 3,700 complaints across more than 11 years were held back from the FDA, which device makers are required to do so within 30 days of reports of patient injuries in addition to investigating them. The company did not begin an internal investigation until 2019. The devices were used by children, the elderly, and over 700,000 U.S. veterans. As many as 15 million devices were affected. People experienced vomiting, dizziness, headaches, and cancers in the lungs, throat, sinuses, and esophagus. Company officials knew about the dangers of the device, but continued to market and sell them.[2]

During the COVID-19 pandemic, the company ramped up production of another ventilator that also included the foam. Operating profits from the ventilators, including the CPAP devices, soared to around US$800 million. During the pandemic, Philips conducted a series of studies on the foam, showing the deteriorating foam and chemicals released by it, which could cause "serious injury, life-threatening or permanent impairment".[2]

The company said patients' health is its top priority, and regretted the "distress and concern" that the recall caused. It said complaints about the foam were limited and were evaluated on a case-by-case basis, and it was made aware of the significance in early 2021, launching the recall soon after. Months after the recall, Philips said that tests showed the chemicals released by the foam were within safe levels.[2]

The company announced a new CPAP machine in April 2021, and soon after admitted that the foam it had used previously had been breaking down in an earnings call. Then-CEO Frans van Houten, in the earnings call, pledged 250 million euros to the problem, and reassured investors that the "device is safe to be continued to use to the best of our knowledge at this time". The company alerted the FDA but not customers. Following the recall, van Houten said he regretted the impact of it on "patients, care providers, and shareholders."[2]

Multiple federal lawsuits have been levied against the company. One settled with the company for US$479 million to reimburse customers.[9][2]

Today[edit]

Philips Respironics's products include devices for the diagnosis and treatment of sleep apnea including CPAP and bi-level (BiPAP) non-invasive ventilation machines, oxygen concentrators for patients requiring supplemental oxygen, infant apnea monitors for infants at risk of SIDS, asthma treatment solutions and hospital ventilators.

References[edit]

  1. ^ "Company Profile for Respironics, Inc (RESP)". Zenobank.com. Archived from the original on July 20, 2010. Retrieved 2008-10-02.
  2. ^ a b c d e f g Cenziper, Debbie; D. Sallah, Michael; Korsh, Michael; Robinson-Johnson, Evan; Sager, Monica (September 27, 2023). "Philips Kept Complaints About Dangerous Breathing Machines Secret While Company Profits Soared". ProPublica. Retrieved October 14, 2023.
  3. ^ "Philips kept complaints about dangerous breathing machines secret while company profits soared". Pittsburgh Post-Gazette Interactive. Pittsburgh Post-Gazette. 27 September 2023. Retrieved 2 February 2024.
  4. ^ "How the CPAP machine beats deadly sleep apnoea". The University of Sydney. Retrieved 2 February 2024.
  5. ^ "Philips recall crisis casts shadow over legacy of Respironics founder". Pittsburgh Post-Gazette. 30 December 2023. Retrieved 2 February 2024.
  6. ^ "ROYAL PHILIPS ELECTRONICS TO ACQUIRE RESPIRONICS FOR USD $66.00 PER SHARE". Respironics. Archived from the original on 10 June 2008.
  7. ^ "PHILIPS ANNOUNCES COMPLETION OF TENDER OFFER TO ACQUIRE RESPIRONICS (EX-99.A.2.I)". www.sec.gov (Press release). 14 March 2008.
  8. ^ Foo Yun Chee; Niclas Mika (2007-12-21). "Philips in $5 billion Respironics deal". Reuters.
  9. ^ Jewett, Christina (September 7, 2023). "CPAP Maker Reaches $479 Million Settlement on Breathing Device Defects". The New York Times. ISSN 0362-4331. Retrieved November 28, 2023.

External links[edit]