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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 they could cause serious health...
2021 Medical Device Recalls | FDA - U.S. Food and …
- https://www.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls
- Dec 16, 2021
2023 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls
- Feb 2, 2023
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 ...
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 …
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, ...
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
- GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients The FDA has identified this as a Class I recall, …
Recalls, Corrections and Removals (Devices) | FDA
- https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices
- In rare instances, where the manufacturer or importer fails to voluntarily recall a device that is a risk to health, FDA may issue a recall order to the manufacturer under 21 CFR 810,...
UPDATE 1-U.S. FDA classifies recall of Philips' respiratory …
- https://finance.yahoo.com/news/1-u-fda-classifies-recall-235951461.html
- 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' respiratory machines as …
Philips CPAP Recall: Related MDRs Top 98K, Including 346 Deaths
- https://www.drugwatch.com/news/2023/02/16/philips-cpap-recall-deaths/
- More than 98,000 medical device reports have been filed with the FDA, including 346 deaths linked to recalled Philips CPAP machines. ... Michelle Llamas has …
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