--- title: "Northeast Scientific Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Northeast Scientific Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/northeast-scientific-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Northeast Scientific Inc. recall records **8** reported ongoing 8 records in this archive. Latest source date Aug 29, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 29, 2025 FDA device enforcement ### [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...](https://isitonrecall.com/recall/fda-device-z-0018-2026-nes-reprocessed-0-9mm-otw-turbo-elite-laser-atherectomy-catheter-model-number-r-410-152-the-nes-repr/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0018-2026%22) Aug 29, 2025 FDA device enforcement ### [NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the...](https://isitonrecall.com/recall/fda-device-z-0019-2026-nes-reprocessed-1-4mm-otw-turbo-elite-laser-atherectomy-catheter-model-number-r-414-151-the-nes-repr/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0019-2026%22) Aug 29, 2025 FDA device enforcement ### [NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the...](https://isitonrecall.com/recall/fda-device-z-0020-2026-nes-reprocessed-1-7mm-otw-turbo-elite-laser-atherectomy-catheter-model-number-r-417-152-the-nes-repr/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0020-2026%22) Aug 29, 2025 FDA device enforcement ### [NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the...](https://isitonrecall.com/recall/fda-device-z-0021-2026-nes-reprocessed-2-0mm-otw-turbo-elite-laser-atherectomy-catheter-model-number-r-420-006-the-nes-repr/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NE...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0021-2026%22) Aug 29, 2025 FDA device enforcement ### [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...](https://isitonrecall.com/recall/fda-device-z-0022-2026-nes-reprocessed-0-9mm-rx-turbo-elite-laser-atherectomy-catheter-model-catalog-number-r-410-154-the-n/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0022-2026%22) Aug 29, 2025 FDA device enforcement ### [NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the ...](https://isitonrecall.com/recall/fda-device-z-0023-2026-nes-reprocessed-1-4mm-rx-turbo-elite-laser-atherectomy-catheter-model-number-r-414-159-the-nes-repro/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0023-2026%22) Aug 29, 2025 FDA device enforcement ### [NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the ...](https://isitonrecall.com/recall/fda-device-z-0024-2026-nes-reprocessed-1-7mm-rx-turbo-elite-laser-atherectomy-catheter-model-number-r-417-156-the-nes-repro/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0024-2026%22) Aug 29, 2025 FDA device enforcement ### [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 ...](https://isitonrecall.com/recall/fda-device-z-0025-2026-nes-reprocessed-2-0mm-rx-turbo-elite-laser-atherectomy-catheter-model-number-r-420-159-the-nes-repro/) Potential for breaches in the sterile barrier packaging, compromising sterility assurance. Class II Reported ongoing Distribution: US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA. [Official source for NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. The NES...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0025-2026%22) ## Reasons in these listed records - Potential for breaches in the sterile barrier packaging, compromising sterility assurance. These examples come from this result page and are not a ranking of every recall reason. ## Checking Northeast Scientific Inc. ### Is there a recall on northeast scientific inc. right now? This archive contains 8 records, including 8 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Northeast Scientific Inc.](https://isitonrecall.com/check/?q=Northeast%20Scientific%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)