Medtronic recalls all Abre Venous Self-Expanding Stent Systems due to reports of stent migration. Learn if your device is affected and what to do.
There have been reports of stent migration.
Medtronic is recalling all versions of its Abre Venous Self-Expanding Stent System because of reports of stent migration. This could cause serious complications if the stent moves inside the body.
Stent migration occurs when the stent moves from its intended position in the body. This can lead to blockages, infections, or other complications that require additional medical intervention.
Patients who have received the Abre Venous Self-Expanding Stent System are most at risk. The recall applies to all model numbers and serial numbers produced by Medtronic.
Check if your device is labeled as the Medtronic Abre Venous Self-Expanding Stent System. All model numbers and serial numbers are included in the recall.
Look for the product name and model numbers on the device or its packaging.
Reach out to Medtronic directly to confirm if your device is affected and get guidance on next steps.
No, this recall specifically applies to the Abre Venous Self-Expanding Stent System only.
Check the device label for the Medtronic Abre Venous Self-Expanding Stent System name and model numbers.
Contact Medtronic directly to confirm if your device is affected and get guidance on next steps.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0464-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0464-2022 from Medtronic. 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.
