Smiths Medical Recalls PneuPac paraPAC Plus Ventilator Kits
The recall follows reports of a malfunction that could lead to insufficient ventilation. The recalled ventilators are used in emergency and transport situations.
The recall follows reports of a malfunction that could lead to insufficient ventilation. The recalled ventilators are used in emergency and transport situations.
Medline Industries is voluntarily recalling several lots and SKUs of tracheostomy care and cleaning trays.
Philips argued in court that its US subsidiary should be responsible for damages caused by its CPAP machines and ventilators, but patients’ attorneys say safety decisions were made at the Dutch company’s highest levels.
Mallinckrodt Manufacturing is recalling its one-way valve, 22F x 22M, due to devices not opening properly, which prevents or reduces the flow of ventilated air or oxygen.
Read MorePhilips has reached an agreement to resolve all economic loss claims related to Philips Respironics’ recall of certain respiratory care and sleep devices.
Read MoreHamilton 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 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 MoreDräger Carina sub-acute care ventilators have been recalled to address possible contamination of the breathing gas, the FDA reports.
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 recall was issued due to a misalignment of the check valve in the device’s manifold, which may cause the manifold to fail and interrupt therapy to neonates.
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 MoreThe recall is due to a container defect that may result in failure to deliver the recommended dose.
Read MoreThe FDA is providing information on oxygenator devices used in extracorporeal circulation following a recall notice by Getinge/Maquet.
Read MoreDraeger Medical is recalling the Seattle PAP Plus as well as VentStar and other breathing circuit/anesthesia kits after finding that glued connections may loosen before or during ventilation due to a manufacturing error.
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