Recently Recalled Medical Devices

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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...

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/

2 days 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 …

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

See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date …

Medical Device Recalls - Food and Drug Administration

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

Feb 13, 2023

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' …

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,...

Recall List: Major Medical Device & Drug …

https://www.drugwatch.com/news/2021/01/05/top-medical-device-drug-recalls-2020/

Fact Checked. In 2020, the Food and Drug Administration announced several large-scale medical device and drug recalls and two high-profile market …

6 recent medical device recalls - Becker's Hospital Review

https://www.beckershospitalreview.com/supply-chain/6-recent-medical-device-recalls.html

Cordis recalls carotid artery device Cordis has recalled its Precise PRO Rx US Carotid System, a device used to treat patients with narrowed carotid arteries. The …

Recently-Approved Devices | FDA - U.S. Food and Drug …

https://www.fda.gov/medical-devices/device-approvals-denials-and-clearances/recently-approved-devices

Recently-Approved Devices | FDA Recently-Approved Devices The products listed here include some of the newest medical technology available. For each product, you can find …

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