Philips ventilator recall classified as most serious by USFDA
New Delhi: The U.S. Food and Drug Administration on Thursday classified the recall of Philips' breathing devices and ventilators as Class 1, or the most serious type of recall, saying the use of these devices may cause serious injuries or death.The agency said there have been 83 complaints regarding the products used to provide breathing assistance, but no injuries or deaths were reported...
New Delhi: The U.S. Food and Drug Administration on Thursday classified the recall of Philips' breathing devices and ventilators as Class 1, or the most serious type of recall, saying the use of these devices may cause serious injuries or death.
The agency said there have been 83 complaints regarding the products used to provide breathing assistance, but no injuries or deaths were reported for these issues.
Read also: Cadila Healthcare arm recalls Metformin Hydrochloride ER tablets in US
The Dutch medical equipment company recalled some of its breathing devices and ventilators in June, as the foam used to dampen the machines' sound could degrade and emit small particles that irritate airways. The gases released may also be toxic or carry cancer risks, Philips had said.
Read also: Trouble for JnJ: Carcinogen found in some Aveeno, Neutrogena sunscreens, products recalled
Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement/treatment or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2024 Minerva Medical Treatment Pvt Ltd