Medtronic Vascular recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk. Affected units may have stainless steel wires exposed, risking injury during procedures.
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, which could cause injury during medical procedures. This recall affects certain models sold with specific serial numbers.
The catheter's primary segment material may deteriorate, exposing underlying stainless steel wires. This could lead to injury if the wires snag or cause damage during medical procedures.
Healthcare professionals using the recalled catheters for cardiovascular procedures are most at risk. Patients receiving these catheters during procedures may also be affected.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F ERAD LEFT, LONG TIP, .070", and reference number SA6ERADLLT. The product was sold with specific lot and serial numbers.
Identify the model, size, and reference number to confirm if your catheter is affected.
The recall indicates a potential risk, so affected units should not be used until the remedy is applied.
Check the product details to see if it matches the recalled model. If affected, contact Medtronic Vascular for guidance.
Look for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F ERAD LEFT, LONG TIP, .070", and reference number SA6ERADLLT. Check the lot and serial numbers on the product.
We’ve drafted a message you can send Medtr: Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2674-2019 — Medtr: Vascular Medtr: Vascular Hello, I own a Medtr: Vascular that is covered by recall Z-2674-2019 from Medtr: Vascular. 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.
