Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models for potential wire exposure. Learn what to do if you own this device.
There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.
Medtronic Vascular is recalling a specific type of cardiovascular catheter due to a risk of internal wires becoming exposed. This could lead to complications during medical procedures.
The catheter's primary segment material may break off, exposing the underlying stainless-steel wires. This could cause damage to blood vessels or other tissues during medical procedures.
Healthcare professionals using this catheter for procedures. Patients receiving the catheter during treatment are at risk if the device is used improperly.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F AL3.0, .070", and reference number SA6AL30. The product was sold with GTIN 00613994823687.
Identify the model, size, and reference number to confirm if your catheter is affected.
Reach out to Medtronic Vascular for guidance on next steps if you have the recalled catheter.
The recall indicates a potential risk, so it is not recommended for use until further instructions are received from Medtronic Vascular.
Check for the model 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F AL3.0, .070", and reference number SA6AL30.
Contact Medtronic Vascular directly for specific instructions on handling the recalled device.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2679-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2679-2019 from Medtronic Vascular. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.