Medical Device Recall

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. Please note that the FDA...

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 receive email updates on medical device recalls, safety communications, and …

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 is recalling the Nuclear Medicine 600 and 800 Series systems after identifying an issue with two mechanisms that prevent uncontrolled …

What is a Medical Device Recall? | FDA

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

Recalls, Corrections and Removals (Devices) | FDA

https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices

Overview. A recall is a method of removing or correcting products that are in violation of …

Medical Device Recall Information - Philips Respironics …

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator …

Medical Device Recalls - Food and Drug Administration

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

Medical Devices. Databases. This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or …

How Philips' significant respiratory devices recall unfolded

https://www.massdevice.com/how-philips-significant-respiratory-devices-recall-unfolded/

Philips’ first recall notification involved specific Philips bi-level positive airway pressure (bi-level PAP), continuous positive airway pressure (CPAP) and mechanical ventilator …

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 from …

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