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Boston Scientific recalls Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: M006175272080 (edited 1/13/2021)
Recalled April 29, 2020 · FDA recall Z-1735-2020 · Boston Scientific
Hazard
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device · FDA Class II
Units
5 units
Sold at
Nationwide Foreign: Europe, Middle East and Africa, the Americas (North America and South America, Asia Pacific and Japan
Description
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device
Product
Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: M006175272080 (edited 1/13/2021)
Manufacturer(s)
Boston Scientific
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →