Medtronic recalls specific SHERPA NX catheters for potential wire exposure. Learn what to do if you own this device.
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 a specific type of cardiovascular catheter that may expose underlying steel wires. This could cause serious injury if the catheter moves during procedures.
The catheter may lose its outer layer, exposing thin steel wires. These wires could cause injury if the catheter shifts during medical procedures.
Cardiovascular patients undergoing procedures with the recalled catheter model. Patients using the device for medical procedures are most at risk.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F JL4.5 SH, .070", and reference number SA6JL45SH. The device is used for cardiovascular procedures.
Look for the model name, size, and reference number on the catheter packaging or label.
Yes, there is a potential for wire exposure that could cause injury during procedures.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F JL4.5 SH, .070", and reference number SA6JL45SH.
The recall does not specify a remedy, so contact Medtronic 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-2686-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2686-2019 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.
