List Of Recalled Medical Devices

2022 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls

Teleflex Recalls Iso-Gard Filter S for Risk of Splitting or Detaching That May Cause Leakage and Insufficient Air Supply to Patients. 11/01/22. Philips Respironics Recalls Certain Masks for BiPAP ...

2021 Medical Device Recalls | FDA

https://cacmap.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls

Dec 16, 2021

UPDATE: Recalled Philips Respironics Ventilators, …

https://www.fda.gov/medical-devices/safety-communications/update-certain-philips-respironics-ventilators-bipap-machines-and-cpap-machines-recalled-due

Recalled Devices. In June 2021, Philips recalled certain ventilators, BiPAP machines, and CPAP machines (see table below) because of potential health risks.

Medical Device Databases | FDA

https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databases

Apr 6, 2022

Philips Respironics Recalls Certain Ventilators and …

https://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-certain-ventilators-and-bipap-machines-due-potential-health-risks-pe-pur

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 …

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 · Feb 16 (Reuters) - U.S. health regulators on Thursday classified the recall of Dutch medical device maker Philips' respiratory machines as most serious, saying their …

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

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 …

Philips CPAP Recall: Related MDRs Top 98K, Including 346 Deaths

https://www.drugwatch.com/news/2023/02/16/philips-cpap-recall-deaths/

Between April 2021 and Dec. 31, 2022, there have reportedly been 346 deaths related to the medical devices. The MDRs include adverse effects reportedly …

List of Recalled Philips Products | Philips Recall Health …

https://lamblawoffice.com/list-of-recalled-philips-products-health-risks-for-patients-fda-safety-alert/

On June 30, 2021, the FDA issued a Safety Communication document concerning the June 2021 recall of certain Philips CPAP machines, BiPAP devices, and …