Fda Recall Medical Device

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 ...

Medical Device Recalls - Food and Drug Administration

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

2023 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls

2022 Medical Device Recalls. Device Name. Date. Smiths Medical Recalls Certain CADD System Administration Sets and Cassette Reservoirs for Issues Causing …

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

11/01/22. Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue with Magnets That May Affect Certain Medical Devices. 10/18/22. Jiangsu …

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, …

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

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. ... See Medical Device …

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 · The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' respiratory machines as most serious, saying …

What is a Medical Device Recall? | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/what-medical-device-recall

Removal - Addresses a problem with a medical device by removing it from where it is used or sold. FDA uses the term “recall” when a manufacturer takes a correction or removal …

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' …