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Boston Scientific Corporation recalls Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intrav
Recalled February 27, 2019 · FDA recall Z-0852-2019 · Boston Scientific
Hazard
A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires. · FDA Class II
Units
49 units
Sold at
Nationwide distribution to AR, CT, FL, IA, IL, IN, KY, MA, MI, ND, NJ, NY, OH, OK, PA, SC, TX, VA, WI, WY.
Description
A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires.
Product
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
Manufacturer(s)
Boston Scientific Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →