FDAAugust 29, 2025device

NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions.

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

00850044399055

Recall history

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

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NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. — Recall Details · AllClear