medical Class II Updated 2019-02-27

Boston Scientific Corporation recalls Stingray" Guidewire, labeled as 300cm. intended to facilita

Recalled 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).

Hazard / Issue

A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Material Number (UPN) H749M3004A0, Batch Number 21558994, Expiration Date 11/30/2019
View official government recall

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