Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn if your catheter is affected and what to do.
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 cause serious complications during medical procedures if the catheter is used improperly.
The catheter's primary segment material can become exposed, revealing stainless-steel braid wires. This may cause injury during medical procedures if the catheter is used without proper handling.
Healthcare professionals using the catheter for cardiovascular procedures are most at risk. Patients receiving the catheter during procedures may also be affected.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, 3DRC 100CM, .070", and reference number SA63DRC. The product was sold with a specific GTIN: 00613994823823.
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 your catheter is recalled.
The recall indicates a potential risk, so it is not recommended for use until the manufacturer provides guidance.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, 3DRC 100CM, .070", and reference number SA63DRC.
Contact Medtronic Vascular directly for specific instructions on handling the recalled item.
We’ve drafted a message you can send Medtr: Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2564-2019 — Medtr: Vascular Medtr: Vascular Hello, I own a Medtr: Vascular that is covered by recall Z-2564-2019 from Medtr: 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.
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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.
