Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential for stainless-steel wire exposure. Affected units may require replacement.
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 stainless-steel wires becoming exposed. This could lead to complications during medical procedures if the catheter is used improperly.
The catheter's primary segment material could become exposed, revealing underlying stainless-steel braid wires. This may cause unintended tissue damage or complications during medical procedures.
Medical professionals who use the SHERPA NX ACTIVE GUIDING CATHETER for cardiovascular procedures are most at risk. Patients receiving this catheter during procedures may also be affected.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, EBU3.75 SH, .070", and reference number SA6EBU375SH. The product was sold with a GTIN of 00613994823540.
Identify the model, size, and reference number to confirm if your catheter is affected.
The recall indicates a potential risk, but the catheter may still be safe if used correctly. Affected units should be replaced per the recall.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, EBU3.75 SH, .070", and reference number SA6EBU375SH.
We’ve drafted a message you can send Medtr: a short, human brand name for headings (e.g. "Trsmima") to request your refund or repair — edit it as you like.
Subject: Recall Z-2668-2019 — Medtr: a short, human brand name for headings (e.g. "Trsmima") Medtr: a short, human brand name for Hello, I own a Medtr: a short, human brand name for headings (e.g. "Trsmima") that is covered by recall Z-2668-2019 from Medtr: a short, human brand name for headings (e.g. "Trsmima"). 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.
