Us Fda Medical & Radiation Emitting Device Recalls

Medical Device Recalls | FDA - U.S. Food and Drug …

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

If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. Please note that the FDA...

Medical Device Recalls - Food and Drug Administration

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

2022 Medical Device Recalls | FDA - U.S. Food and …

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 …

Radiation-Emitting Products | FDA - U.S. Food and Drug …

https://www.fda.gov/radiation-emitting-products

In May 2022, the FDA announced organizational changes within CDRH, including the creation of OHT8. Navigate the Radiation-Emitting Products Sesection Radiation …

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, …

Alerts and Notices | FDA

https://www.fda.gov/radiation-emitting-products/radiation-safety/alerts-and-notices

FDA Statement on Radiation Overexposures in Panama Consumer Safety Alert: Internet Sales of Laser Products Ultraviolet Radiation Burns from High Intensity Metal Halide and …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/textsearch.cfm

Device Classification; FDA Guidance Documents ; Humanitarian Device Exemption ; Medsun Reports; Premarket Approvals (PMAs) Post-Approval Studies; …

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...

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 …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/ressimplesearch.cfm

Medical Device Recalls Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary …