Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible 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. The catheters may expose underlying steel wires, which could cause serious injury if the catheter moves inside the body.
The catheter's outer layer may break off, exposing the inner steel wires. If the catheter shifts during use, these wires could damage blood vessels or cause bleeding.
Cardiovascular doctors and medical facilities using the recalled catheters are most at risk. Patients undergoing procedures with these catheters could face complications.
Check for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, MPH, 55CM, 070", REF SA6MPHK. The product was sold with GTIN 00613994823076 and all lot/serial numbers.
Identify the model and GTIN to confirm if your catheter is recalled.
The recall states there is a potential risk of wire exposure, so it is not safe to use without checking the recall details.
Check for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, MPH, 55CM, 070", REF SA6MPHK. The product was sold with GTIN 00613994823076 and all lot/serial numbers.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2598-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2598-2019 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.