Murilo Freitas – Página 3

FDA Takes Steps to Ensure Safety of Cinnamon Products Sold in the US

Murilo Freitas - 20:28, 5 de marzo de 202494

FDA Takes Steps to Ensure Safety of Cinnamon Products Sold in the US
http://www.fda.gov/news-events/press-announcements/fda-takes-steps-ensure-safety-cinnamon-products-sold-us

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Baxter Healthcare Recalls ExactaMix Pro 1200 and Pro 2400 Due to a Software Error

Murilo Freitas - 05:00, 5 de marzo de 202473

Baxter Healthcare is recalling the ExactaMix Pro 1200 and Pro 2400 for a software error causing potential over-delivery of ingredients in the final solution.

http://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-recalls-exactamix-pro-1200-and-pro-2400-due-software-error

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FDA Roundup: March 5, 2024

Murilo Freitas - 22:37, 4 de marzo de 202485

FDA Roundup: March 5, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-5-2024

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FDA Clears First Over-the-Counter Continuous Glucose Monitor

Murilo Freitas - 21:21, 4 de marzo de 202439

FDA Clears First Over-the-Counter Continuous Glucose Monitor
http://www.fda.gov/news-events/press-announcements/fda-clears-first-over-counter-continuous-glucose-monitor

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Smiths Medical ASD Inc. Recalls Medfusion Model 3500 Syringe Pump Due to Issues Associated with Earlier Software Versions

Murilo Freitas - 05:00, 4 de marzo de 202474

Smiths Medical recalls Medfusion 3500 syringe pump due to software issues affecting delivery alarms, infusion restarts, screen locks, and critical functions.

http://www.fda.gov/medical-devices/medical-device-recalls/smiths-medical-asd-inc-recalls-medfusion-model-3500-syringe-pump-due-issues-associated-earlier

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FDA Roundup: March 1, 2024

Murilo Freitas - 20:58, 29 de febrero de 202495

FDA Roundup: March 1, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-march-1-2024

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Potential Exposure to Certain Chemicals with Use of GE HealthCare EVair and EVair03 Compressors with Certain Ventilators – Letter to Health Care Providers

Murilo Freitas - 05:00, 29 de febrero de 2024168

FDA issues a letter to health care providers on potential exposure to certain chemicals with use of GE HealthCare EVair and EVair03 compressors with certain ventilators.

http://www.fda.gov/medical-devices/letters-health-care-providers/potential-exposure-certain-chemicals-use-ge-healthcare-evair-and-evair03-compressors-certain

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Datex-Ohmeda Recalls EVair Air Compressors Due to Formaldehyde Emissions Found in Specific Conditions When Used with CARESCAPE R860, Engstrom Carestation or Pro Ventilators

Murilo Freitas - 05:00, 29 de febrero de 202492

EVair Air compressors recalled due to increased formaldehyde emissions at high temperature and low gas flow conditions when used with certain ventilators.

http://www.fda.gov/medical-devices/medical-device-recalls/datex-ohmeda-recalls-evair-air-compressors-due-formaldehyde-emissions-found-specific-conditions-when

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Megadyne Medical Products, Inc. Recalls Mega Soft Universal Patient Return Electrode Due to Reports of Patient Burns

Murilo Freitas - 05:00, 29 de febrero de 2024172

Megadyne is updating the instructions and product labeling to reflect that the Mega Soft Universal pads should not be used in patients under 12 years old.

http://www.fda.gov/medical-devices/medical-device-recalls/megadyne-medical-products-inc-recalls-mega-soft-universal-patient-return-electrode-due-reports

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Follow Instructions for Safe Use of Electrical Operating Room Tables – Letter to Health Care Providers

Murilo Freitas - 05:00, 28 de febrero de 2024109

Problems may occur if electrical operating room table best practices are not followed. Read the FDA’s recommendations to avoid complications.

http://www.fda.gov/medical-devices/letters-health-care-providers/follow-instructions-safe-use-electrical-operating-room-tables-letter-health-care-providers