Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER 6F models 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 CATHETER models used in cardiovascular procedures. The recall is because a subset of these catheters may have stainless steel wires exposed, which could cause injury during medical procedures.
The catheter's primary segment material may degrade, exposing stainless steel braid wires. This could lead to injury if the catheter is used during medical procedures.
Healthcare professionals using the catheter 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 6F', reference number 'SA6AL75A', and the GTIN 00613994823960. All lot and serial numbers are affected.
Identify the model, reference number, and GTIN to confirm if your catheter is affected.
The recall states there is a potential for wire exposure, but the exact risk level is not specified in the record.
Check for the model 'SHERPA NX ACTIVE GUIDING CATHETER 6F', reference number 'SA6AL75A', and GTIN 00613994823960.
The recall record 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-2568-2019 — 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-2568-2019 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.
