Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible exposure of stainless steel wires, risking injury 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 heart procedures because a small section of the catheter could break off, exposing metal wires inside. This could cause injury if the catheter is used improperly.
The catheter's outer layer may break off during use, exposing the internal stainless steel wires. This could cause injury if the wires move inside the body or interact with medical equipment.
Cardiovascular doctors and medical staff who use the recalled catheters for procedures. Patients undergoing these procedures are at risk if the catheter is used without proper safety checks.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F ECR4.0 SH, .070", and reference number SA6ECR40SH. The product was sold with a GTIN: 00613994824813.
Identify the model, size, and reference number 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 if it's recalled.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
Look for the model 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F ECR4.0 SH, .070", and reference number SA6ECR40SH.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2692-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2692-2019 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.
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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.
