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Boston Scientific Corporation recalls ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston Scie

Recalled January 27, 2021 · FDA recall Z-0870-2021 · Boston Scientific

Hazard
Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters distributed in the US that did not undergo the applicable sterile processing procedure. · FDA Class II
Units
5 units
Sold at
US Nationwide distribution including in the states of Tulsa, OK.

Description

Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters distributed in the US that did not undergo the applicable sterile processing procedure.

Product
ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston Scientific coronary venous lead is positioned.
Manufacturer(s)
Boston Scientific Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Boston Scientific Corporation recalls ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston Scie | RecallWatchUSA