Recall
FDAHealthAugust 29, 2025

Northeast Scientific Inc. — 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 us

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 29, 2025

US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA.

What's affected?

Product
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.
Lot code
that

Additional details

Model No R-410-152; UDI-DI 00850044399055; All Lot Numbers that are within their labeled shelf life with expiration dates prior to 29AUG2026

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 561 units.

View original FDA notice →

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