Fda Medical Recalls

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

2022 Medical Device Recalls | FDA 2022 Medical Device Recalls The list below contains recalls that were issued in 2022. 2022 Medical Device Recalls

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

2023 Medical Device Recalls | FDA An official website of the United States government Here’s how you know U.S. Food and Drug Administration Search Menu …

Medical Device Recalls - Food and Drug Administration

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

Recalls, Market Withdrawals, & Safety Alerts | FDA

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

A Terminated Recall is a recall where the FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the …

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 · Follow. Feb 16 (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' (PHG.AS) …

Drug Recalls | FDA

https://www.fda.gov/drugs/drug-safety-and-availability/drug-recalls

A Terminated Recall is a recall where the FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the …

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, …

FDA Dashboards - Recalls - Food and Drug Administration

https://datadashboard.fda.gov/ora/cd/recalls.htm

Recalls Recalls NEW! Compliance Actions data is now available through RESTful APIs on the FDA Data Dashboard. Caveats: Certain information in these datasets may not be …