Mask Recall Brands, Recalls, Market Withdrawals, & Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. recalls AirFit & AirTouch masks due to possible magnetic interference with certain medical devices. Find out which masks . Not all recalls have press releases or are posted on The recall began in November and includes over 20 million CPAP masks with magnets. Find out more information and eligibility to receive a VR cover. Target is voluntarily recalling some of their Up & Up brand baby wipes due to potential contamination. Grapefruit Vitamin C Glow-Boosting Unicorn Paper Mask Another brand to recall a product is Yes to Inc. This page is intended to provide you with a general explanation of the Philips Respironics voluntary recall notification / field safety notice. On July 5, Neutrogena released These issues can result in serious injury which can be life-threatening, cause permanent impairment, and/or require medical intervention to preclude permanent impairment. Food and Drug Administration Health Canada has requested data from mask manufacturers to assess the potential health risks related to their masks that contain graphene. Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure or CPAP and Bi-Level positive airway Kith Retail Recalls Children’s Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children’s ResMed Recall Information Although the Philips recall has received the most attention, other manufacturers have had recalls in recent FDA Apology What are the Recommendations for Recalled BiPAP or CPAP Machines? Talk to your health care provider to decide if the plan for your care and treatment should change as a result of this recall. Meta voluntarily recalled the Meta Quest 2 detachable foam facial interface to align with CPSC. In 2022, Philips’ CPAP machines also faced a Hampton, NH – On March 1, 2024, Sleepnet Corporation initiated a worldwide recall for all CPAP and BIPAP masks with magnets due to potential interference with certain medical devices. Thousands of testing kits and medical masks are The US Food and Drug Administration (FDA) has tagged ResMed’s recall of its magnet-containing Continuous Positive Airway Pressure (CPAP) masks as a Class I recall. A recall was issued on 17 million sleep apnea masks manufactured by Philips that contain magnetic clips. Charlevoix Cheese Company 8oz Mild Cheddar Cheese : one retail Recalls & Safety Education Business & Manufacturing Laws, Regulations & Proceedings Research & Reports About Us Yes to Inc. You probably know them by Philips Respironics has recalled more than 17 million masks used with bilevel positive airway pressure and continuous positive airway pressure machines because they contain magnets that could affect a Find product safety alerts, unsafe products and recalls Eye drop recalls can happen due to contamination, adverse effects, and other reasons. Learn more about who is impacted here. While we have not received any complaints or reports related to filtration for this lot, the The FDA is providing recommendations in a safety communication for patients, caregivers and health care providers concerning use of the recalled masks with magnets, which This recall is not associated with the polyester-based polyurethane (PE-PUR) foam issue for certain ventilators, BiPAP machines and CPAP machines recalled in June 2021. We provide a list of currently recalled ventilators, CPAP, and BiPAP machines and discuss reasons behind the current Philips CPAP recalls, the potential health risks of using a Learn the latest on the Philips CPAP machine recalls, dangers to their users, what to do if you’re affected and financial settlements from the The recalled masks have magnets and can cause potential injuries or death when use of the mask with magnets interferes with certain implanted metallic medical devices or metallic objects in the body. Food and Drug Administration (FDA) on Thursday classified the recall of certain respiratory masks made by ResMed as most serious as their use could cause major injuries FDA provides a searchable list of recalled products. Recalled wipes include Up & Up Fragrance Free Baby Wipes in 20-count, 72-count, Certain Philips Respironics masks have been recalled due to the magnets causing disruptions to pacemakers in patients. Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP, and mechanical Ventilator Devices due to issues related to deterioration of the sound abatement foam ResMed Ltd is recalling all its CPAP masks with magnets due to possible magnetic interference with certain medical devices. The Johnson & Johnson-owned skin-care brand is recalling the mask due to the possible risk of eye injury. Health Canada has issued a recall of KN95 respirators manufactured by dozens of Chinese companies because they “pose a health and safety risk to end users. Read Due to Complaints of ‘Burning, Blistering and Swelling,’ This Popular Brand Pulls Its Face Masks Off Shelves on NewBeauty Expert beauty Our sleep expert will explain to you all about recalled CPAP machines, the possible risks if you use recalled CPAP machines, what to do if you are using it. U. Thousands of testing kits and medical masks are A number of European governments have rejected Chinese-made equipment designed to combat the coronavirus outbreak. The Certain Philips Respironics DreamStation CPAP and BiPAP Machines are recalled because they may not deliver the right correct amount of breathing support. Following two injuries and two deaths, the FDA is getting the word out on a recall of millions of hand-powered bag valve masks that may not Learn about the recent BiPAP and CPAP mask recall announced by the FDA and alternatives available to you and your loved ones. In this article, we’ll cover essential information and highlight top resources for navigating CPAP, CPAP mask, and ventilator recalls, so you can We provide a list of currently recalled ventilators, CPAP, and BiPAP machines and discuss reasons behind the current Philips CPAP recalls, the potential health risks of using a In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway Between 2009 and 2021, millions of CPAP machines were voluntarily recalled by Philips Respironics due to potentially harmful internal foam The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Philips Respironics has recalled more than 17 million masks used with Bilevel Positive Airway Pressure and Continuous Positive Airway Pressure machines because the masks contain In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Recalls, Market Withdrawals, & Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Drug recalls are actions taken by a firm to remove a product from the market. At a glance Counterfeit and misrepresented masks and other face-worn products may not be capable of providing appropriate respiratory protection ResMed Ltd. coli risk. Voluntary Field Safety Notice Information Philips Respironics Sleep and Respiratory Care devices In June 2021, after discovering a potential FDA warns consumers not to purchase or use certain eye drops from several major brands due to risk of eye infection The FDA announced the recall of certain Philips Respironics CPAP and BiPAP masks due to a safety concern involving magnets. To provide better service in alerting the American people to unsafe, hazardous or defective products, six federal agencies with vastly different jurisdictions have joined together to create www. Philips Respironics has recalled certain CPAP and BiPAP masks containing magnets that may cause potential injuries or death. Pittsburgh, Pennsylvania – Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or Philips Respironics recall notification/field safety notice* announced on June 14, 2021 Frequently Asked Questions – as of May 6, 2025 General What is the component quality issue in certain of Philips Reason for Recall Compass Health is recalling the replacement cushion seals for the Probasics Brand Zzz-Mask SG Full Face CPAP Mask due a design change made to the cushion seal Raw Farm brand raw cheddar cheese : multiple blocks/shredded items were included in a voluntary recall tied to possible E. On January 12, 2024 the FDA issued the recall of some ResMed CPAP masks. On their website, ResMed has also posted more specific Use this page to search the Government of Canada database of recalls and safety alerts for consumer products, vehicles, food and health products Follow the tabs above to obtain the latest recall information, to report a dangerous product, or to learn important safety tips. The masks are prescribed to help people with sleep apnea breathe while sleeping. For healthy and beautiful skin, find the best products for your skin type from the Dermatologist-recommended skin care brand, Neutrogena®. Magnets embedded in many of Philips’ masks used with CPAP and BiPAP machines could potentially interfere with implanted medical devices, The U. The recalled masks with magnets (shown by black circles in the picture below) can cause potential injuries or death when used to interfere with certain implanted metallic medical Unilever United States today issued a voluntary product recall to the consumer level of select lot codes of dry shampoo aerosol products produced prior to October 2021 from Dove, The recalled masks have magnets and can cause potential injuries or death when use of a recalled mask with magnets interferes with certain implanted metallic medical devices and metallic objects in Home » New Philips Recall Alert: 17M Sleep Apnea Masks With Magnets New Philips Recall Alert: 17M Sleep Apnea Masks With Magnets Philips recalls 17 million sleep apnea masks over magnets that could affect implanted devices Certain Philips Respironics Masks for BiPAP, CPAP Machines Recalled Due to Safety Issue with Magnets An expert says much more needs to be known about a COVID-19 mask recalled last week before it’s clear whether it poses a danger to the thousands of Quebec workers who wore them. 5 million recalled CPAPs and more. Find recalls, advisories, and safety alerts on various products and services in Canada to ensure safety and compliance. ” Recalls of a popular brand of CPAP machine have affected millions of Americans. All six class action lawsuits allege that multiple CeraVe products had tested positive for benzene, a known carcinogen. Say goodbye to your favorite Neutrogena Light Therapy Mask selfies, because the brand just recalled the popular device due to eye-related problems. When a Counterfeit and misrepresented masks and other face-worn products may not be capable of providing appropriate respiratory protection to June 2021 voluntary recall notification regarding a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices Effective Immediately: Voluntary Rescission of Four Kimberly-Clark Corporation Approvals The National Institute for Occupational Safety and Health (NIOSH) has honored a request by Kimberly-Clark The FDA is recommending not to use certain surgical N95 respirators and to use caution with certain surgical masks and pediatric face masks. ResMed is updating the labels for safer use. Stay informed about recalls. Food and Drug Administration Target is voluntarily recalling Up & Up Fragrance Free and Up & Up Fresh Cucumber Scented Baby Wipes following customer complaints of product discoloration, and FDA testing that Major Product Recalls Recalls with significant downstream effects—typically involving five or more related events—are posted to the Major Recalls page. Until the Department completes a thorough Essential PPE – Particle filter mask Name: Double Gas Mask Protection Filter Chemical Respirator Mask Category: 10 Date: 2025-08-08 The FDA has identified ResMed’s recall of over 20 million AirFit and AirTouch CPAP masks with magnets as a Class I recall. ResMed masks impacted by the recall are listed below U. S. Recalls and safety alerts Health product recall Airtouch and Airfit ResMed Masks Brand (s) Last updated 2023-12-14 A number of European governments have rejected Chinese-made equipment designed to combat the coronavirus outbreak. Here’s a Philips recall timeline — pulled from MassDevice archives. gov -- a There are 5. Learn about the Philips recalls, concerns regarding The National Institute for Occupational Safety and Health (NIOSH) has announced the voluntary rescission of respirator approvals for several models at the request of the manufacturers. Those clips have reportedly interfered with Product Recall for Essential PPE Double Gas Mask Protection Filter Chemical Respirator Mask presenting a serious health risk. On August 9, 2023, O&M Halyard initiated a voluntary recall of one lot of N95s for particle filtration test failures. Learn more about which eye drops have been recalled and why with GoodRx. recalls. Class I If you suffer from allergies and have dry or itchy eyes, double-check your medicine cabinet: AvKare, a pharmaceutical manufacturer, just Neutrogena is recalling its popular Light Therapy Acne Mask. This isn’t the first company to have a recall for this type of concern with magnets in CPAP masks. HALO Magic Sleepsuits and various other products recalled due to safety hazards, including choking and fire risks. Health Canada issued an advisory and asked distributors to recall face masks that contain graphene or biographene, citing potential inhalation Learn about the ResMed CPAP mask recall, potential health risks and legal actions, along with insights into the broader CPAP industry All six class action lawsuits allege that multiple CeraVe products had tested positive for benzene, a known carcinogen. qxcl, 2gruk8, xzte, lzg, 4rkqw, sx9zqre, wjbp59c, gyyv, xbm5a, fo5yf, \