Device Recalls And Medical

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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/

1 day ago · Feb 16 (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' (PHG.AS) respiratory machines as most serious, saying...

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

The FDA posts summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that …

GE HealthCare Recalls Nuclear Medicine Systems for …

https://www.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

Device Use GE Nuclear Medicine 600 and 800 Series systems are used by health care professionals to evaluate diseases, trauma, abnormalities, and disorders. …

Yale-led study urges action by Congress to close FDA …

https://www.ctpublic.org/news/2023-02-16/yale-led-study-urges-congress-action-to-close-fda-loophole-permitting-dangerous-medical-devices

2 days ago · The Yale study, in collaboration with Harvard Medical School, analyzed a number of medical devices that eventually issued Class I recalls. “If the FDA authorizes …

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 …

Recalls, Corrections and Removals (Devices) | FDA

https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices

You must contact your FDA’s Office of Regulatory Affairs (ORA) Division Recall Coordinator (DRC) listed here by state or region (look for Product Type “Medical Device”). Foreign …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm

This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or removal actions initiated …

Philips CPAP Recall: Related MDRs Top 98K, Including 346 Deaths

https://www.drugwatch.com/news/2023/02/16/philips-cpap-recall-deaths/

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 CPAP recalls …

Smiths Medical Recalls Certain CADD System …

https://www.fda.gov/medical-devices/medical-device-recalls/smiths-medical-recalls-certain-cadd-system-administration-sets-and-cassette-reservoirs-issues

For additional information or technical assistance, you can contact Smith Medical’s Technical Assistance at 1- (800)-258-5361. Additional Resources: Medical …

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