FDADecember 3, 2019device
Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW System Console.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A loose ODU plug / Coaxial cable connection may result in fluctuating flow values on the Console.
What to do
FDA enforcement status: Terminated
Brands named
maquet cardiovascular us salesmaquetmaquet cardiovascular
UPCs
04037691258997
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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