Medtronic recalls specific models of Ascenda Intrathecal Catheters (8780, 8781, 8784) due to a design update that may lead to tissue growth in the catheter connector, potentially causing occlusion. Affected units have unique serial numbers listed in the recall.
Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead to catheter occlusion.
Medtronic is recalling specific models of Ascenda Intrathecal Catheters (8780, 8781, and 8784) because a design update could allow tissue to grow into the catheter connector, which might block the catheter and cause problems. This is a minor risk that doesn't require immediate action but should be checked.
The design update aims to reduce tissue growth into the catheter connector, but in some cases, tissue can still grow into the connector, potentially blocking the catheter and causing occlusion. This is a minor risk that doesn't typically lead to serious injury.
Patients using Medtronic Ascenda Intrathecal Catheters with the specified model numbers and serial numbers listed in the recall are most at risk. The risk is low and unlikely to cause serious injury.
Check if your catheter has model numbers 8780 (114 cm), 8781 (140 cm), or 8784 (catheter pump revision kit). Affected units have specific serial numbers listed in the recall document.
Identify if your catheter is model 8780, 8781, or 8784 by checking the label on the device.
Compare your serial number with the list of affected serial numbers provided in the recall notice.
Models 8780 (114 cm), 8781 (140 cm), and 8784 (catheter pump revision kit) are affected.
No, this is a low-risk issue that doesn't require immediate action. However, you should check if your catheter is affected and review the serial numbers.
You should review the list of affected serial numbers and contact Medtronic for further instructions.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2352-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2352-2024 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.
