GE Healthcare ventilator batteries recall classified most serious by USFDA

GE Healthcare, the medical device making arm of General Electric, had initiated the recall of 4,222 of its ventilator batteries distributed between April 2, 2019, and April 18, 2022.

Published On 2022-06-29 08:30 GMT   |   Update On 2022-06-29 08:30 GMT

New Delhi: U.S. health regulators on Tuesday classified the recall of some backup batteries of GE Healthcare's ventilators, which the company had initiated in mid-April, as the most serious type, saying that their use could lead to injuries or death.The CARESCAPE R860 ventilator's backup batteries, including replacement backup batteries, were recalled as they were running...

Login or Register to read the full article

New Delhi: U.S. health regulators on Tuesday classified the recall of some backup batteries of GE Healthcare's ventilators, which the company had initiated in mid-April, as the most serious type, saying that their use could lead to injuries or death.

The CARESCAPE R860 ventilator's backup batteries, including replacement backup batteries, were recalled as they were running out earlier-than-expected, which could cause the device to shut down preventing the patient from receiving breathing support, the U.S. Food and Drug Administration said.

The CARESCAPE R860 ventilators use the main power via a wall plug to operate and the device's backup battery is meant to keep it running in situations such as patient transport.

GE Healthcare, the medical device making arm of General Electric, had initiated the recall of 4,222 of its ventilator batteries distributed between April 2, 2019, and April 18, 2022. 

There have been 1,553 complaints and one injury associated with the use of the device, the FDA said.

Read also: Baxter International lung therapy devices recall classified most serious by USFDA

On Tuesday, Philips said independent tests on ventilators that the Dutch company recalled last year because of possible health risks showed the problems were almost exclusively caused by unauthorized cleaning products.

The Amsterdam-based company's recall was launched amid concerns that a type of foam used in the devices could deteriorate and become toxic

Read also: Dr Shravan Subramanyam named as new MD, President and CEO of GE Healthcare, India and South Asia

Tags:    
Article Source : Reuters

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

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News