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 during medical procedures.
The catheter's primary segment material may break off, exposing the underlying stainless-steel wires. This could lead to complications like kinking or blockages during procedures.
Patients and medical professionals who use the recalled catheter for cardiovascular procedures are affected. Those with the specific model and lot numbers are most at risk.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, JR4.0, 110CM, 070", and reference number SA6JR40A. The product was sold with a specific GTIN: 00613994822314.
Identify the model, size, and reference number to confirm if your catheter is recalled.
The recall indicates a potential risk only in specific circumstances, not all use.
Check for the model 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F, JR4.0, 110CM, 070", and reference number SA6JR40A.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
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-2592-2019 — 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-2592-2019 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.
