The FDA has received more than 100 reports of deaths associated with popular sleep aid devices many relied on worldwide.
So many sleep apnea patients across the globe relied on the devices covered under the recall that Philips said it did not have enough parts to repair or replace devices immediately, leaving some patients without many options.
Coleman said he’s still waiting on a replacement device, and since learning of the recall, he’s now sleeping without any sleep-aid device after weighing the risks, but he worries for other veterans out there who may not know about the problem. The FDA told NBC 5 Responds it is looking into each report, but felt it was important to share the preliminary findings with the public.
The company said, “Philips regrets any inconveniences caused by this issue and we are committed to supporting the community of patients who rely on our sleep and respiratory care solutions.”Frank Reese is one of millions of sleep apnea patients now concerned for their health after learning of a recall on their Philips CPAP machines.published by the American Journal of Respiratory and Critical Care Medicine last December that found patients using its devices did not have a higher risk of cancer.
The subpoena from the DOJ was “to provide information related to events leading to the Respironics recall,” van Houten said. “The relevant subsidiaries are cooperating with the agency.”
United States Latest News, United States Headlines
Similar News:You can also read news stories similar to this one that we have collected from other news sources.
FDA Chief to Detail Delays Inspecting Baby Formula PlantThe head of the Food and Drug Administration is preparing to tell lawmakers about events that led to a months-long gap before inspecting the plant at the center of a nationwide baby formula shortage. FDA Commissioner Robert Califf is scheduled to answer questions Wednesday from House lawmakers probing the formula shortage. According to prepared testimony, Califf will tell lawmakers that a COVID-19 outbreak at Abbott’s formula plant led regulators to delay their inspection from late December to January. Califf will also discuss delays in interviewing an Abbott whistleblower who alleged serious violations at the baby formula plant last October.
Read more »
FDA head will explain holdups in inspection of baby formula facility amid shortageFDA chief Robert Califf will address concerns from Congress about the nationwide baby formula shortage as lawmakers investigate the details of what led to the shortage.
Read more »
FDA chief to detail delays inspecting baby formula plantThe head of the Food and Drug Administration is preparing to tell lawmakers about events that led to a months-long gap before inspecting the plant at the center of a nationwide baby formula shortage.
Read more »
FDA Chief to Detail Why Inspection of Baby Formula Plant Was DelayedThe head of the Food and Drug Administration is preparing to tell lawmakers about events that led to a months-long gap before inspecting the plant at the center of a nationwide baby formula shortage.
Read more »
U.S. FDA declines to authorize Verrica's viral skin disease treatmentThe U.S. Food and Drug Administration (FDA) declined to approve Verrica Pharmaceuticals Inc's drug for the treatment of a viral skin disease known as molluscum contagiosum, the company said on Tuesday.
Read more »
Colorado Congresswoman Diana DeGette To Grill Baby Formula Manufacturers, FDA Over ShortageColorado Congresswoman Diana DeGette is leading a federal inquiry into the nation's baby formula shortage. DeGette is the Chair of the House Energy and Commerce Committee's Oversight and Investigations Subcommittee. She is also a new grandmother who understands the sense of panic and urgency gripping parents.
Read more »