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Northeast Scientific Inc. Recalls

8 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Northeast Scientific Inc..

8Total Recalls
0Critical
4,194Units Affected
Aug 29, 2025Most Recent
All Recalls

Every Northeast Scientific Inc. Recall

Sorted by most recent. Click any recall for full details.

8 recalls
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Athere...
Surgical Devices·616 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NES Reprocessed Turbo-Elite Laser Ather...
Surgical Devices·199 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. The NES Reprocessed Turbo-Elite Laser Athere...
Surgical Devices·141 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-Elite Laser Ather...
Surgical Devices·561 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NES Reprocessed Turbo-Elite Laser At...
Surgical Devices·173 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Athere...
Surgical Devices·1,019 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. The NES Reprocessed Turbo-Elite Lase...
Surgical Devices·795 affected·Aug 29, 2025
High RiskFDA
Northeast Scientific Inc.
NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood vessels of the perip...
Surgical Devices·690 affected·Apr 26, 2021