Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch of 185cm Stingray Guidewires are incorrectly...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Boston Scientific Corporation directly.
Affected Products
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).
Quantity: 49 units
Why Was This Recalled?
A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm guidewires.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Boston Scientific Corporation
Boston Scientific Corporation has 601 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report