Maquet Cardiovascular Us Sales, Llc recalls Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model N
Recalled Product
Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW System Console.
Hazard / Issue
A loose ODU plug / Coaxial cable connection may result in fluctuating flow values on the Console.
Issued by
FDA
Affected States: ME, NV, NY, OH, PA, TX, VA
Lot/Code Info: UDI: 04037691258997; Serial Numbers 9348936 910114412 910114420 910114429 910114430 910114432 910114435 910114438 910117243 91064722 91067680
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