Boston Scientific recalls Innova Self-Expanding Stent Systems (200mm) with material numbers H74939293052030 to H74939293082070 due to possible failure to fully release from delivery system.
Stent possibly unable to be fully released from the delivery system.
Boston Scientific is recalling specific models of Innova Self-Expanding Stent Systems (200mm) because they may not fully release from the delivery system. This could lead to improper placement in blood vessels during medical procedures.
The stent may not fully release from the delivery system during medical procedures, potentially causing improper placement in blood vessels. This could lead to complications like blockages or damage to the artery.
Patients who received the recalled stent systems during vascular procedures are likely affected. Medical professionals using these stents for treatment of leg artery conditions are at highest risk.
Check for material numbers H74939293052030 through H74939293082070 on the stent packaging. The product is used for leg artery treatments and comes in sizes 5x200x130, 5x200x75, 6x200x130, and other variants.
Look for material numbers H74939293052030 to H74939293082070 on the stent packaging or documentation.
Reach out to Boston Scientific directly for guidance on next steps if you have the recalled stent.
The recalled stents are Innova Self-Expanding Stent Systems (200mm) with material numbers H74939293052030 to H74939293082070.
The stent may not fully release from the delivery system during medical procedures, potentially causing improper placement in blood vessels.
Check for material numbers H74939293052030 through H74939293082070 on the stent packaging or documentation.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0685-2018 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0685-2018 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.
