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 device malfunctions during use.
The catheter's primary segment material may break off, exposing the stainless-steel braid wires. This could lead to serious injury if the wires cause damage to blood vessels or tissues during a procedure.
Cardiovascular professionals who use these catheters for procedures are most at risk. Patients undergoing procedures with the recalled catheters could face complications.
Check for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, MB1, 90CM, 070", REF SA6MB1D. The product was sold with a specific GTIN: 00613994821959.
Verify the model number and serial number against the recall list provided by Medtronic.
The recall states there is a potential for wire exposure, so users should check if their catheter is affected before use.
The recall does not specify a remedy, so contact Medtronic directly for guidance.
Look for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, MB1, 90CM, 070", REF SA6MB1D. The product was sold with GTIN: 00613994821959.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2596-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2596-2019 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.