Medtronic Vascular recalls SHERPA NX Active Guiding Catheters (6F AL2.0) due to potential wire exposure. 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 certain SHERPA NX Active Guiding Catheters for cardiovascular use. The catheters could expose underlying stainless steel wires, which might cause injury during medical procedures.
The catheter's primary segment material may break off, exposing the stainless steel braid wires. This could lead to injury if the wires snag or cause damage during procedures.
Cardiovascular professionals using the recalled catheters are most at risk. Patients undergoing procedures with these catheters could face injury if wires become exposed.
Check for the model SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. The product was sold with GTIN 00613994823731 and all lot/serial numbers.
Identify the model SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. with GTIN 00613994823731.
The recall indicates a potential risk of wire exposure, so it is not safe to use without checking the recall details.
The official recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
Look for the model SHERPA NX ACTIVE GUIDING CATHETER, 6F AL2.0, .070", REF SA6AL20. with GTIN 00613994823731 and all lot/serial numbers.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2623-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2623-2019 from Medtronic 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.
