Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models 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 Vascular is recalling a specific type of cardiovascular catheter due to a risk of internal wires becoming exposed, which could cause serious complications. This affects patients who have received this catheter during procedures.
The catheter's primary segment material may break off, exposing the underlying stainless-steel braid wires. This could lead to complications like tissue damage or blockages if the wires become embedded in the body.
Patients who have received the recalled catheter during cardiovascular procedures are most at risk. The recall applies to specific model numbers and sizes used in medical settings.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, JL3.5, 110CM, 070", and reference number SA6JL35A. The product was sold for cardiovascular use in medical settings.
Medtronic Vascular will provide details on how to report the catheter if you have it.
The recall indicates a potential risk, so it is not safe to use without contacting Medtronic Vascular first.
Look for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, JL3.5, 110CM, 070", and reference number SA6JL35A.
Contact Medtronic Vascular to report the catheter and get instructions on next steps.
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-2588-2019 — 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-2588-2019 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.
