CPAP
BIRMINGHAM, Alabama (April 25, 2022)—Philips expects to produce and ship more than 90% of new or repaired devices to consumers to replace their recalled CPAP, BiPAP and mechanical ventilators by the end of 2022, the company said Monday.
CINCINNATI (April 21, 2022)—Quipt Home Medical Corp., a United States-based leader in the home medical equipment industry, focused on end-to-end respiratory care, announced that it has acquired Good Night Medical, LLC, a business with operations across seven U.S. states, for approximately $7 million in Cash.
PHOENIX (March 29, 2022)—Fisher & Paykel Healthcare (F&P) will be showing off its wares at Booth #621 at Medtrade West, scheduled to begin on Monday, April 4 at the Phoenix Convention Center. The Auckland, New Zealand-based F&P recently reported that the company expects full year operating revenue for the 2022 financial year to be in the range of $1.675 billion to $1.70 billion.
PHILADELPHIA (March 24, 2022)—Philips was hit with a potential class action last week by a medical device retailer claiming it and others are owed a refund due to lost money because they were unable to resell Philips' CPAP and BiPAP breathing machines, which contained PE-PUR foam.
PLYMOUTH MEETING, Penn. (February 25, 2022)—AdaptHealth Corp., a provider of patient-centered, health care-at-home solutions including home medical equipment, medical supplies and related services, announced financial results for the fourth quarter and fiscal year ended Dec. 31, 2021.
ST. LOUIS (January 11, 2022)—Responsive Respiratory (RRI) recently released a new Product Solutions catalog.
This comprehensive oxygen catalog highlights RRI’s newest entry into the sleep market, the Purify O3 Elite Sanitizer, as well as its commitment to high pressure oxygen products.
KANSAS CITY, Mo. (November 30, 2021)— Advanced Medical Resources is now distributing the Resvent iBreeze line of CPAPs in the United States. Resvent received Emergency Use Authorization from the Food and Drug Administration (FDA), and is seeking 510K clearance. The three units Advanced Medical Resources is offering include model 20A Auto CPAP, model 25STA Auto BiPAP ST and model 30STA Auto BiPAP SV.
BIRMINGHAM, Ala. (November 16, 2021)—During a recent plant inspection, the Food & Drug Administration (FDA) found that silicone-based foam Philips Respironics planned to use to repair recalled CPAP and ventilator devices had failed a safety test for volatile organic compounds.
DEERFIELD BEACH, Fla. (November 5, 2021)—As America prepares to observe Veterans Day in honor of those who served, fought and died for us, AirAvant Medical and First Nation Group announce a partnership alliance providing the FDA-cleared Bongo Rx Expiratory Positive Airway Pressure (EPAP) device to vterans and active-duty military members suffering from obstructive sleep apnea (OSA).
PETERBOROUGH, N.H. (October 13, 2021)—SoClean Inc. today announced that it has filed a federal lawsuit in the United States District Court for the District of Massachusetts against Philips, the maker of continuous positive airway pressure (CPAP) and bi-level positive airway pressure (BiPAP) devices.
FREMONT, Neb. (October 7, 2021)—Kubat HealthCare, a health care service provider, announced the acquisition of Miller Pharmacy Specialties located at 322 E 22nd St, Fremont, Nebraska, 68025.
ATLANTA (September 7, 2021)—In mid-August, the United States’ Department of Justice (DOJ) reported that Kevin Rumph, Jr., 41, of Fairburn, Georgia, pleaded guilty to a charge of theft of medical products. Rumph used his U.S. Department of Veteran Affairs (VA) issued credit card to buy over $1.9 million worth of continuous positive airway pressure (CPAP) equipment, which he stole and then sold.
PORT WASHINGTON, N.Y. (September 1, 2021)—Drive DeVilbiss Healthcare announced today the discontinuation of the DV5 and DV6 series CPAP devices as of December 2021. As a result, Drive DeVilbiss will no longer accept new CPAP orders in order to fill as many open orders as possible.
AMSTERDAM (September 1, 2021)—Royal Philips today announced an update in connection with the June 14, 2021 recall notification for specific Philips sleep and respiratory care devices that was issued to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices. More than half of the affected devices in use globally are in the United States. The vast majority (>80%) of the registered affected devices in the U.S.
WASHINGTON, D.C. (August 26, 2021)—On August 25, the Centers for Medicare & Medicaid Services (CMS) distributed an alert on Philips respiratory products under recall. In their notice, CMS tells patients with recalled devices:
WATERLOO, Iowa (August 23, 2021)—VGM Fulfillment, a division of VGM & Associates, is proud to announce the opening of a new warehouse location is Shiremanstown, Pennsylvania. The new warehouse will open on Sept. 7, 2021, and once it reaches full capacity will employ approximately 40 people. The warehouse provides 108,000 square feet of space.
SAN DIEGO (August 16, 2021)—ResMed, a provider of digital health and sleep apnea treatment, launched AirSense 11, available first in the United States, the company’s next-generation PAP (positive airway pressure) device designed to help hundreds of millions of people worldwide with sleep apnea start and stay on therapy to treat and manage obstructive sleep apnea.