Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk during cardiovascular procedures.
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 is recalling certain SHERPA NX Active Guiding Catheters used in cardiovascular procedures due to a risk of internal wire exposure. This could lead to complications if the catheter is used improperly.
The catheter may lose its primary segment material, exposing stainless-steel braid wires. This could cause complications during procedures if the wires become exposed.
Cardiovascular professionals who use the recalled catheters for procedures are affected. Patients receiving these catheters during procedures may also be at risk.
Check for the model SHERPA NX ACTIVE GUIDING CATHETER, 6F JL3.0, .070", REF SA6JL30. with GTIN:00613994822260. All lot and serial numbers are included in the recall.
Identify the model, size, and reference number to confirm if your catheter is recalled.
The recall states there is a potential risk, so it is not recommended for use until the remedy is applied.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
Look for the model SHERPA NX ACTIVE GUIDING CATHETER, 6F JL3.0, .070", REF SA6JL30. with GTIN:00613994822260.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2620-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2620-2019 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.