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FDA Approves New Therapy for Rare Form of Blood Cancers Called Myelodysplastic Syndromes

Murilo Freitas - 19:51, 23 de octubre de 2023227

FDA Approves New Therapy for Rare Form of Blood Cancers Called Myelodysplastic Syndromes
http://www.fda.gov/news-events/press-announcements/fda-approves-new-therapy-rare-form-blood-cancers-called-myelodysplastic-syndromes

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FDA Roundup: October 24, 2023

Murilo Freitas - 18:25, 23 de octubre de 2023231

FDA Roundup: October 24, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-october-24-2023

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Fresenius Medical Care Recalls Some Hemodialysis Machines for Potential Exposure to Toxic Compounds

Murilo Freitas - 04:00, 23 de octubre de 2023225

Fresenius Medical Care 2008 Series Hemodialysis Machines are recalled for the potential for toxic compounds leaching from chlorinated peroxide cured silicone tubing.

http://www.fda.gov/medical-devices/medical-device-recalls/fresenius-medical-care-recalls-some-hemodialysis-machines-potential-exposure-toxic-compounds

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FDA Roundup: October 20, 2023

Murilo Freitas - 18:25, 19 de octubre de 2023227

FDA Roundup: October 20, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-october-20-2023

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Philips Respironics Recalls V60 and V60 Plus Ventilators due to Power Management Printed Circuit Board Assemblies (PM PCBAs) Not Meeting Ventilator Standards

Murilo Freitas - 04:00, 19 de octubre de 2023224

Philips Respironics recalls V60 and V60 Plus Ventilators because the PM PCBAs do not conform with ventilators standards.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-v60-and-v60-plus-ventilators-due-power-management-printed-circuit-board

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FDA Deputy Commissioner for Human Foods Commits to Fulfilling Vision of Proposed Program

Murilo Freitas - 13:21, 18 de octubre de 2023321

FDA Deputy Commissioner for Human Foods Commits to Fulfilling Vision of Proposed Program
http://www.fda.gov/news-events/press-announcements/fda-deputy-commissioner-human-foods-commits-fulfilling-vision-proposed-program

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Medtronic Notification of Stolen Defective Products – Potentially Defective McGRATH™ MAC Video Laryngoscopes

Murilo Freitas - 04:00, 18 de octubre de 2023220

Medtronic is issuing this notification to inform the public of stolen defective McGRATH™ MAC video laryngoscopes that have been offered for sale illegally by unauthorized third parties through various social media platforms. These affected products did not pass Medtronic’s rigorous quality tests est

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medtronic-notification-stolen-defective-products-potentially-defective-mcgrathtm-mac-video

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Hamilton Medical Inc. Recalls HAMILTON-C1, T1, MR-1 Ventilators for Capacitator Leaks and Short Circuits

Murilo Freitas - 04:00, 17 de octubre de 2023281

Hamilton recalls their HAMILTON-C1, T1, MR-1 ventilators for capacitators that may leak electrolyte onto the control board and cause short circuiting.

http://www.fda.gov/medical-devices/medical-device-recalls/hamilton-medical-inc-recalls-hamilton-c1-t1-mr-1-ventilators-capacitator-leaks-and-short-circuits

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Do Not Use Tests Manufactured by Universal Meditech, Inc.: FDA Safety Communication

Murilo Freitas - 04:00, 17 de octubre de 2023361

Universal Meditech, Inc has notified FDA that it has stopped all operations. Their tests should not be used.

http://www.fda.gov/medical-devices/safety-communications/do-not-use-tests-manufactured-universal-meditech-inc-fda-safety-communication

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FDA Roundup: October 17, 2023

Murilo Freitas - 19:34, 16 de octubre de 2023276

FDA Roundup: October 17, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-october-17-2023