Recalled Medical Devices

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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 · 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) respiratory machines as most serious ...

Medical Device Recalls | FDA

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. …

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 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

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, …

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 ...

Philips recalls certain reworked Trilogy, Garbin ventilators

https://www.massdevice.com/philips-recalls-reworked-trilogy-garbin-ventilators/

1 day ago · The FDA notice includes devices distributed between March 1, 2022, and Sept. 6, 2022. Devices recalled in the U.S. total 13,811 since Philips initiated the recall on …

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

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

The U.S. Food and Drug Administration reported that it has received more than 98,000 medical device reports related to machines named in Philips CPAP recalls …

Philips Respironics CPAP, BiPAP, and Ventilator Recall: …

https://www.fda.gov/medical-devices/safety-communications/faqs-philips-respironics-ventilator-bipap-machine-and-cpap-machine-recalls

Philips Respironics (Philips) voluntarily recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and …

2023 Medical Device Recalls | FDA

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

Feb 2, 2023

The Deadly Medical Devices That Were Recalled In 2020

https://www.brownbarron.com/blog/2021/may/the-deadly-medical-devices-that-were-recalled-in/

May 25, 2021

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