FDAAugust 29, 2025device

NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for market...

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

The hazard

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

What to do

FDA enforcement status: Ongoing

Brands named

northeast scientificnortheast

UPCs

00850044399062

Recall history

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

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