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Ventilator Correction: Philips Updates Use Instructions for Trilogy Evo, EvoO2, EV300, Evo Universal, Aeris EVO, Garbin Evo, and LifeVent EVO2 due to Risk of Inaccurate Flow Measurements Caused By Certain In-Line Nebulizer Placements

Murilo Freitas - 05:00, 18 de November de 2024100
Inline nebulizers in certain configutations on Trilogy Evo continuous ventilators may lead to inaccurate flow measurements which may cause patient injury.

http://www.fda.gov/medical-devices/medical-device-recalls/ventilator-correction-philips-updates-use-instructions-trilogy-evo-evoo2-ev300-evo-universal-aeris

 
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Battery Pack Correction: Smiths Medical Updates Use Instructions for CADD-Solis Li-ion Rechargeable Battery Packs Due to Risk That Pack Damage May Cause a Circuit Short and Prevent Recharge

Murilo Freitas - 05:00, 18 de November de 2024103
Battery casing damage on CADD-Solis battery packs, which provide alternate power to infusion pumps, may cause a circuit short and prevent recharging.

http://www.fda.gov/medical-devices/medical-device-recalls/battery-pack-correction-smiths-medical-updates-use-instructions-cadd-solis-li-ion-rechargeable

 
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Endoscopic Vessel Harvesting System Recall: Getinge and Maquet Cardiovascular Remove VasoView HemoPro 1 and 1.5 Endoscopic Vessel

Murilo Freitas - 05:00, 14 de November de 2024124
HemoPro EVH Systems are being recalled due to a risk for silicone to detach from the device and enter the patient during minimally invasive surgery.

http://www.fda.gov/medical-devices/medical-device-recalls/endoscopic-vessel-harvesting-system-recall-getinge-and-maquet-cardiovascular-remove-vasoview-hemopro

 
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