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Cardiac Assist, Inc recalls TandemHeart Pump Kit, Product: 5120-0000 - Product Usage: provides temporary extracorporeal circulatory system support
Recalled May 20, 2020 · FDA recall Z-1948-2020 · Cardiac Assist
Hazard
Failure to prime due to an assembly error · FDA Class II
Units
10
Sold at
US Nationwide distributions.
Description
Failure to prime due to an assembly error
Product
TandemHeart Pump Kit, Product: 5120-0000 - Product Usage: provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.
Manufacturer(s)
Cardiac Assist, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →