FDAFebruary 22, 2021device

EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT100S,SterileEO, Rx Only, UDI: 00812499030006

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

The hazard

It has been identified that the catheter size on the packaging labeling does not correspond to the widest part of the catheter. In addition the IFU contains the incorrect diameter of the catheter. This could result in blood stagnation, clots or air emboli.

What to do

FDA enforcement status: Ongoing

Brands named

epix therapeuticsepix

UPCs

00812499030006

Recall history

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

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