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Northeast Scientific Recalls
9 recalls on record · September 1, 2021 to October 8, 2025 · Medical Devices
Recalls by year
21
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. The NES Reprocessed Turbo-E
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-E
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-E
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. The NES Reprocessed
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NES Reprocessed Turbo-
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NES Reprocessed Turbo-
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NES Reprocessed Tur
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
October 8, 2025Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-
Hazard: Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
September 1, 2021Medical DevicesFDA
Northeast Scientific Inc. recalls NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood ves
Hazard: 510k indicated one (1) reprocessing cycle, product not cleared for additional reprocessing cycles.