Boston Scientific recalls Contour VL Variable Length Ureteral Stents with nickel debris from manufacturing. Affected models include UPN M0061801550-1570. Consumers should contact for details.
Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.
Boston Scientific is recalling certain Contour VL Variable Length Ureteral Stents due to trace nickel debris found during manufacturing. This could cause irritation or infection if the stent is implanted. The recall affects specific model numbers and production lots.
Trace nickel particles were found in the stent during manufacturing. These particles could cause irritation or infection if the stent is implanted in the ureter. The risk is low but requires medical attention if symptoms occur.
Patients who received the recalled stents during surgery are most at risk. The recall applies to specific model numbers and production lots sold between 2018 and 2020.
Check the product model numbers: UPN M0061801550, M0061801560, or M0061801570. Look for production lots listed in the recall notice: 25578577, 25598812, and other specific numbers.
Reach out to Boston Scientific for details about your specific stent model and production lot.
The recall is for stents with trace nickel debris found during manufacturing. If you have the recalled model, contact Boston Scientific for medical advice.
Check the product model numbers: UPN M0061801550, M0061801560, or M0061801570. Look for production lots listed in the recall notice.
Contact Boston Scientific directly for details about your specific stent model and production lot to determine next steps.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0757-2021 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0757-2021 from Boston Scientific. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
