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Breathing Circuit Kit Recall: Sentec/Percussionaire Removes VDR4 Phasitron Breathing Circuits due to Venturi Component Malfunctions that May Reduce Pressure and Volume Flow

Murilo Freitas - 05:00, 9 de February de 2025183
Phasitron Breathing Circuits support continuous ventilation. A malfunctioning venturi component in the circuit may cause reduced oxygen flow.

http://www.fda.gov/medical-devices/medical-device-recalls/breathing-circuit-kit-recall-sentecpercussionaire-removes-vdr4-phasitron-breathing-circuits-due

 
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Arterial Catheter Recall: Medline Industries, LP, Removes Integrated Arterial Catheters due to Excess Material at Catheter Hub that May Detach

Murilo Freitas - 05:00, 5 de February de 2025229
Medline Integrated Arterial Catheters continuously monitor blood pressure. Excess material on the catheter hub that may detach and enter the patient.

http://www.fda.gov/medical-devices/medical-device-recalls/arterial-catheter-recall-medline-industries-lp-removes-integrated-arterial-catheters-due-excess

 
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Continuous Ventilator Correction: Baxter Healthcare Corporation Issues Correction for Life2000 Ventilator due to a nonconforming battery charger, which triggers a battery alarm and renders the ventilator inoperable

Murilo Freitas - 05:00, 4 de February de 2025140
Baxter Healthcare is recalling the Life2000 Ventilator System by correction, due to a defective battery charger making the ventilator inoperable.

http://www.fda.gov/medical-devices/medical-device-recalls/continuous-ventilator-correction-baxter-healthcare-corporation-issues-correction-life2000-ventilator

 
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FDA Alerts Patients to Regularly Check Diabetes-Related Smartphone Device Alert Settings, Especially Following Phone Hardware or Software Changes

Murilo Freitas - 05:00, 4 de February de 2025144
The FDA is alerting users of diabetes-related medical devices that smartphones connected to diabetes devices may fail to send critical safety alerts.

http://www.fda.gov/medical-devices/safety-communications/fda-alerts-patients-regularly-check-diabetes-related-smartphone-device-alert-settings-especially

 
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Oxygen Concentrator Recall: JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD Removes JMC5A Ni/TruAire-5 Oxygen Concentrator due to the devices spontaneously catching fire

Murilo Freitas - 05:00, 4 de February de 2025179
JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD is recalling certain devices due to incidents of device melting and fire during the use of oxygen concentrators.

http://www.fda.gov/medical-devices/medical-device-recalls/oxygen-concentrator-recall-jiangsu-jumao-x-care-medical-equipment-co-ltd-removes-jmc5a-nitruaire-5

 
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