Murilo Freitas – Página 6

FDA Approves First Medication to Help Reduce Allergic Reactions to Multiple Foods After Accidental Exposure

Murilo Freitas - 16:57, 15 de febrero de 2024305

FDA Approves First Medication to Help Reduce Allergic Reactions to Multiple Foods After Accidental Exposure
http://www.fda.gov/news-events/press-announcements/fda-approves-first-medication-help-reduce-allergic-reactions-multiple-foods-after-accidental

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Philips Recalls BrightView Imaging Systems Due to the Detector Unexpectedly Falling

Murilo Freitas - 05:00, 14 de febrero de 2024304

If the detector support component fails, imaging cannot be completed, and the detector may contact the patient.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-recalls-brightview-imaging-systems-due-detector-unexpectedly-falling

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FDA Approves First Medication to Treat Severe Frostbite

Murilo Freitas - 14:15, 13 de febrero de 2024307

FDA Approves First Medication to Treat Severe Frostbite
http://www.fda.gov/news-events/press-announcements/fda-approves-first-medication-treat-severe-frostbite

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Smiths Medical ASD Inc. Recalls Medfusion Model 4000 Syringe Pump Due to Issues Associated with Earlier Software Versions

Murilo Freitas - 05:00, 13 de febrero de 2024288

Smiths Medical recalls Medfusion model 4000 syringe pump due to software issues, impacting the alarm system, pump, control screen, and other components.

http://www.fda.gov/medical-devices/medical-device-recalls/smiths-medical-asd-inc-recalls-medfusion-model-4000-syringe-pump-due-issues-associated-earlier

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FDA Roundup: February 13, 2024

Murilo Freitas - 17:38, 12 de febrero de 2024326

FDA Roundup: February 13, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-13-2024

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FDA Roundup: February 9, 2024

Murilo Freitas - 20:36, 8 de febrero de 2024277

FDA Roundup: February 9, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-9-2024

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FDA Roundup: February 6, 2024

Murilo Freitas - 20:41, 5 de febrero de 2024312

FDA Roundup: February 6, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-6-2024

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Percussionaire Recalls High Frequency Transport Phasitron Breathing Circuit Kits for Over-Pressurization

Murilo Freitas - 05:00, 5 de febrero de 2024274

The High Frequency Transport Phasitron Breathing Circuit Kit is used for continuous ventilation of patients. The kits are recalled due to a product defect that causes over-pressurization.

http://www.fda.gov/medical-devices/medical-device-recalls/percussionaire-recalls-high-frequency-transport-phasitron-breathing-circuit-kits-over-pressurization

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Cardinal Health Issues Medical Device Recall for Nurse Assist Products Contained Within Kits/Trays

Murilo Freitas - 05:00, 4 de febrero de 2024248

In direct response to the Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urolo

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cardinal-health-issues-medical-device-recall-nurse-assist-products-contained-within-kitstrays-0

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Today The World Issues Voluntary Nationwide Recall of All Lots of Arize Herbal Dietary Supplement Capsules Due to the Presence of Undeclared Nortadalafil

Murilo Freitas - 05:00, 4 de febrero de 2024400

“Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level.
FDA analysis has found the products to contain undeclared Nortadalafil (structurally similar to Tadalafil). Nortadalafil is an active drug ingredient known for treatment of male ere

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/today-world-issues-voluntary-nationwide-recall-all-lots-arize-herbal-dietary-supplement-capsules-due