Breas Medical Issues Correction for Ventilator Due to Formaldehyde Risk
Breas Medical has issued a nationwide correction for Vivo 45 LS ventilators due to potential short-term formaldehyde exposure.
Breas Medical has issued a nationwide correction for Vivo 45 LS ventilators due to potential short-term formaldehyde exposure.
Medtronic will discontinue its Puritan Bennett ventilator series, including the Puritan Bennett 980, Puritan Bennett 840, and Puritan Bennett 560 ventilators.
The 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
Hamilton Medical is recalling the Hamilton-C1, C2, C3, and T1 ventilators after receiving reports of software issues that may cause the ventilators to stop without notice.
Read MoreThe FDA has identified Draeger’s recall for its Carina sub-acute care ventilators as a Class I recall, the most serious type.
Read MoreThe new distribution partnership is expected to help mitigate industry-wide issues with ventilator availability.
Read MorePhilips is recalling Trilogy Evo, Evo O2, EV300, and Evo Universal ventilators after detecting dust and dirt from the environment in the air path of some devices, according to an FDA advisory dated Aug 14, 2023.
Read MoreIntroducing the Puritan Bennett™ PB980: the future of ICU ventilation. Redefining safety and efficiency, it’s a game-changer for respiratory care. Delve deeper with our white paper.
Read MoreExor NV, a Netherlands-based diversified holding company, has bought a 15% stake in Royal Philips, with an option to increase it to 20%.Â
Read MoreDräger Carina sub-acute care ventilators have been recalled to address possible contamination of the breathing gas, the FDA reports.
Read MoreRT looks at the latest ventilators and critical care products on the market from manufacturers Bio-Med Devices, Breas Medical, Dräger, Getinge, Movair, Turn Medical, and Zoll.
Read MorePhilips Respironics provided an update on the field action for specific sleep therapy and ventilator devices involved in the company’s ongoing recall.
Read MoreThe FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Read MoreDräger has received 510(k) clearance from the US FDA for its Evita V600, V800, and Babylog VN800, ventilators.
Read MoreServo-air Lite offers ICU-quality ventilation but is more geared toward spontaneously breathing patients in need of extra breathing support, according to Getinge.
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