Medtronic recalls Endurant Stent Graft System model ENTF2525C70EE due to spindle detachment risk during deployment. Affected units have specific serial numbers and GTIN code.
During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube
Medtronic is recalling the Endurant Stent Graft System model ENTF2525C70EE because the spindle may detach during deployment, potentially causing complications. This recall affects patients who have received this specific medical device.
During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube. This could lead to complications if the device malfunctions during the procedure.
Patients who received the Endurant Stent Graft System model ENTF2525C70EE from Medtronic are most at risk. The recall applies to specific units with serial numbers V30624638 and V30624639.
Check for the model number ENTF2525C70EE on the device packaging or documentation. Affected units have serial numbers V30624638 or V30624639 and GTIN code 00763000006129.
Verify the model number and serial numbers on the device packaging or documentation to confirm if it is affected.
The recalled model is ENTF2525C70EE.
The affected units have serial numbers V30624638 and V30624639.
The recall record does not specify a remedy.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0290-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0290-2022 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.
