FDAAugust 22, 2019device

CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-10002, a component of the CentriMag Extracorporeal Blood Pumping System.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Reports have been received of the CentriMag Systems experiencing motor and pump issues resulting from electromagnetic interference (EMI).

What to do

FDA enforcement status: Terminated

Brands named

thoratec switzerlandthoratec

UPCs

07640135140078

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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