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Maquet Cardiovascular Us Sales, Llc recalls Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW
Recalled December 18, 2019 · FDA recall Z-0678-2020 · Maquet Cardiovascular Us Sales
Hazard
A loose ODU plug / Coaxial cable connection may result in fluctuating flow values on the Console. · FDA Class II
Units
11 distributed in the US
Sold at
The products were distributed to the following US states: ME, NV, NY, OH, PA, TX, and VA.
Description
A loose ODU plug / Coaxial cable connection may result in fluctuating flow values on the Console.
Product
Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW System Console.
Manufacturer(s)
Maquet Cardiovascular Us Sales, Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →