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Maquet Cardiovascular Us Sales, Llc recalls Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator
Recalled April 20, 2016 · FDA recall Z-1373-2016 · Maquet Cardiovascular Us Sales
Hazard
Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the potential risk of exposure to endotoxin for various products. · FDA Class II
Units
72,000 units in total
Sold at
US Nationwide Distribution.
Description
Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the potential risk of exposure to endotoxin for various products.
Product
Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator
Manufacturer(s)
Maquet Cardiovascular Us Sales, Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →