FDAAugust 29, 2025device

NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. 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 marketing in t...

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

00850044399086

Recall history

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

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