Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if you own this catheter for 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 Vascular is recalling a specific type of cardiovascular catheter due to a risk of metal wires becoming exposed, which could cause complications during procedures. This is a serious issue for patients undergoing catheter-based treatments.
The catheter's primary segment material can become exposed, revealing stainless-steel braid wires. This could lead to complications during procedures, such as tissue damage or blockages.
Patients who have received this catheter for cardiovascular procedures are most at risk. Healthcare providers using the device for medical treatments may also be affected.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER, 6F SR3.5 SH, .070" REF SA6SR35SH' on the device. This catheter is used for cardiovascular procedures and has a specific GTIN number.
Identify the model name and GTIN number to confirm if your catheter is affected.
The recall indicates a potential risk, so it is not recommended for use without checking the recall details.
Check the model and GTIN number to confirm if it is affected; contact Medtronic Vascular for further instructions.
Look for the model name 'SHERPA NX ACTIVE GUIDING CATHETER, 6F SR3.5 SH, .070" REF SA6SR35SH' and the GTIN number 00613994822789.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2614-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2614-2019 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.
