Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential for wire exposure. Learn if your catheter is affected and what to do.
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, which could cause serious complications. This recall affects catheters with the model number SA6AL15.
The catheter's primary segment material could become exposed, revealing stainless-steel braid wires. This might lead to complications like tissue damage or blockages during procedures.
Healthcare professionals who use this catheter for cardiovascular procedures are most at risk. Patients receiving the catheter during procedures may also be affected.
Check for the model number SA6AL15 on your catheter. The product is used for cardiovascular procedures and has a specific GTIN number.
Look for the model number SA6AL15 on the catheter's label.
The recall states there is a potential risk, so it is not recommended for use until the remedy is applied.
Check for the model number SA6AL15 on the catheter's label.
The recall does not specify a remedy, so contact Medtronic Vascular for further instructions.
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-2659-2019 — 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-2659-2019 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.
