Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific Corporation Due to Trace amounts of metallic debris were found on...
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
Contour VL Variable Length Ureteral Stent, UPN M0061801550, M0061801560, M0061801570
Quantity: 458 units
Why Was This Recalled?
Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.
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