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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
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 safety …
2023 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls
- An official website of the United States government Here’s how you know U.S. Food and Drug Administration Search Menu Home Medical Devices Medical Device …
Medical Device Recalls - Food and Drug Administration
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm
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 …
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 …
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, …
U.S. FDA classifies recall of Philips' respiratory devices as most …
- https://news.yahoo.com/u-fda-classifies-recall-philips-232501854.html
- (Reuters) -The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' respiratory machines as …
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 · February 16, 2023, 6:12 PM · 1 min read. Feb 16 (Reuters) - U.S. health regulators on Thursday classified the recall of Dutch medical device maker Philips' …
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