Northeast Scientific Inc. 2025-10-08 Health serious FDA
Health · FDA · Recall #FDA-Z-0021-2026
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number:… Recall
Issued October 8, 2025 · Northeast Scientific Inc.
In October 2025, Northeast Scientific Inc. recalled the NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number:…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
What you should do
- 1 Stop using NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Northeast Scientific Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Northeast Scientific Inc.
- Category
- Health
- Recall date
- October 8, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA.
- Recall number
- FDA-Z-0021-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Northeast Scientific Inc. has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.