FDAApril 26, 2021device

NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood vessels of the peripheral vasculature by providing a crosssectional image of such vessels. NES Ref. No. R-88901

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

510k indicated one (1) reprocessing cycle, product not cleared for additional reprocessing cycles.

What to do

FDA enforcement status: Terminated

Brands named

northeast scientificnortheast

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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