Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER model 6F MAC3.75 SH for potential wire exposure. Learn what to do if affected.
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 internal wires becoming exposed. This could cause serious complications during medical procedures.
The catheter's primary segment material can break off, exposing the underlying stainless-steel wires. This could lead to complications like kinking or blockages during procedures.
Healthcare professionals using the catheter for procedures. Patients undergoing cardiac interventions may be at risk if the catheter is used.
Check for the model number 6F MAC3.75 SH, size .070", and reference SA6MAC375SH. The product was sold for cardiovascular use with GTIN 00613994822031.
Identify the model number 6F MAC3.75 SH, size .070", and reference SA6MAC375SH on the catheter packaging.
The recall states there is a potential for wire exposure, so it is not safe to use without checking the recall details.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
Check for the model number 6F MAC3.75 SH, size .070", and reference SA6MAC375SH on the packaging.
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-2748-2019 — 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-2748-2019 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.
