Baxter Healthcare Corporation recalls In-Line ventilator adaptor
Recalled Product
In-Line ventilator adaptor
Hazard / Issue
There is a potential of reduced oxygenation or pneumothorax/barotrauma to occur when the Volara system is used with in-line ventilator in home care environment.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: M07937 MODULE, OPTIMUS HANDSET 2; UDI-DI: 00887761984622. Manufacturing dates October 17, 2019 to present.
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