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U.S. FDA classifies recall of Philips' respiratory devices as most ...
- https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-classifies-recall-philips-respiratory-devices-most-serious-2023-02-16/
- 2 days ago · The recall follows Philips' move to call back millions of breathing devices and ventilators in June 2021 due to the potential of a foam part degrading and becoming toxic, possibly causing cancer.
U.S. FDA classifies recall of Philips' respiratory devices as most …
- https://news.yahoo.com/u-fda-classifies-recall-philips-232501854.html
- February 16, 2023, 3:25 PM · 1 min read. (Reuters) -The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker …
Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
- If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …
U.S. FDA classifies recall of Philips' respiratory devices as most …
- https://finance.yahoo.com/news/u-fda-classifies-recall-philips-231246716.html
- 2 days ago · Feb 16 (Reuters) - U.S. health regulators on Thursday classified the recall of Dutch medical device maker Philips' respiratory machines as most serious, saying their …
GE HealthCare Recalls Nuclear Medicine 600/800 …
- https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients
- GE HealthCare is recalling the Nuclear Medicine 600 and 800 Series systems after identifying an issue with two mechanisms that prevent uncontrolled …
Philips CPAP Recall: Related MDRs Top 98K, Including 346 Deaths
- https://www.drugwatch.com/news/2023/02/16/philips-cpap-recall-deaths/
- Fact Checked The U.S. Food and Drug Administration reported that it has received more than 98,000 medical device reports related to machines named in Philips …
2022 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
- 2021 Medical Device Recalls Subscribe to Medical Device Safety and Recalls Sign up to receive email updates on medical device recalls, safety communications, and other …
The Deadly Medical Devices That Were Recalled In 2020
- https://www.brownbarron.com/blog/2021/may/the-deadly-medical-devices-that-were-recalled-in/
- May 25, 2021
Recalls, Corrections and Removals (Devices) | FDA
- https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices
- Recall is a voluntary action that takes place because manufacturers and distributors carry out their responsibility to protect the public health and well-being from products that …
Medical Device Recall Information - Philips …
- https://www.usa.philips.com/healthcare/e/sleep/communications/src-update
- All Affected Devices Manufactured Before 26 April 2021, All Device Serial Numbers Continuous Ventilator, Minimum Ventilatory Support, Facility Use E30 …
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