Baxter Healthcare Corporation recalls Prismaflex Control Unit, software versions below 7.21
Recalled Product
Prismaflex Control Unit, software versions below 7.21
Hazard / Issue
Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Product Code: 114870; All Lot numbers; GTIN: 07332414115395. Device not distributed in the US.
View official government recall
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