FDAFebruary 22, 2021device

EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259

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

00812499030259

Recall history

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

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EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259 — Recall Details · AllClear