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Philips Respironics Recalls Trilogy Evo, Evo O2, EV300, and Evo Universal Ventilators After Finding Dust and Dirt in Air Path That Can Reduce Air Flow to Patients

Philips Trilogy Evo, Evo O2, EV300, and Evo Universal ventilators provide breathing support, but dust and dirt in the air path may impact air flow to patients.

http://www.fda.gov/medical-devices/medical-device-recalls/philips-respironics-recalls-trilogy-evo-evo-o2-ev300-and-evo-universal-ventilators-after-finding

 
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Dräger Issues Worldwide Voluntary Recall Notification for Carina Sub-Acute Care Ventilators to Address Possible Contamination of the Breathing Gas with 1,3-Dichloropropan-2-ol

Drägerwerk AG & Co. KGaA initiated a voluntary recall notification for Dräger Carina Sub-Acute Care Ventilators to address possible contamination of the breathing gas with 1,3-Dichloropropan-2-ol, a constituent of the PE-PUR foam used for sound insulation. To date, Dräger’s market surveillance act

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/drager-issues-worldwide-voluntary-recall-notification-carina-sub-acute-care-ventilators-address

 
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Baxter Healthcare Corporation Recalls SIGMA Spectrum Infusion Pumps with Master Drug Library and Spectrum IQ Infusion Systems with Dose IQ Safety Software for Repeat Upstream Occlusion False Alarms

Software upgrades to the SIGMA Spectrum and Spectrum IQ infusion pumps are leading to an increase in false alarms for upstream occlusion.

http://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-corporation-recalls-sigma-spectrum-infusion-pumps-master-drug-library-and-spectrum