Breas Medical Updates Use Instructions for Vivo 45 LS Ventilators
Internal testing identified the potential for a short-term increase in formaldehyde exposure for people using new ventilators for the first time.
Internal testing identified the potential for a short-term increase in formaldehyde exposure for people using new ventilators for the first time.
Medline issued the recall due to risk of the inflation tube or other components becoming detached or torn from the main tube.Â
A study of critical care patients at a large children's hospital finds unplanned extubations are common and linked to adverse events in nearly half of patients. Researchers identify the top risk factors, informing potential patient safety improvement practices.
Until the requirements of the consent decree are met, Philips Respironics will not sell new CPAP, BiPAP, or other respiratory care devices in the US.
Read MoreResMed is updating its guides for all CPAP masks with magnets to inform users about potential magnetic interference when magnets are near certain implants and medical devices in the body.
Read MoreMedline Industries is voluntarily recalling several lots and SKUs of tracheostomy care and cleaning trays.
Read MoreOlympus Corp is recalling certain bronchofiberscopes and bronchovideoscopes because they may lead to burns or catch fire.
Read MoreGetinge is recalling the Cardiohelp Emergency Drive due to possible blocking or impairment of the emergency drive’s cranking ability.
Read MoreResMed has issued an urgent field safety notice for its CPAP masks with magnets due to potential interference with some implants or certain medical devices.
Read MoreSoClean has issued a voluntary recall of its SoClean2 and SoClean3 equipment used to clean, sanitize, or disinfect CPAP devices and accessories.
Read MoreOlympus announced a voluntary field corrective action to address complaints of endobronchial combustion occurring during therapeutic procedures involving use of high-frequency therapy equipment in an oxygenated environment.
Read MoreMillions of people were impacted by the 2021 recall of Philips breathing machines. Here are nine of their stories.
Read MoreMedtronic issued a notification to inform the public of stolen defective video laryngoscopes that have been offered for sale illegally by unauthorized third parties through social media platforms.Â
Read MoreThe ventilators contain power management printed circuit board assemblies that were distributed by a third-party warehouse and do not meet ventilator standards, per a safety communication.Â
Read MoreFor patients in the pediatric ICU, pulse oximetry and waveform capnography are valuable tools to monitor the effectiveness of respiratory support and to inform treatment decisions.
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