Medtronic recalls specific SHERPA NX Active Guiding Catheters for possible wire exposure risk. Affected units have a potential for stainless steel wires to become exposed, requiring immediate action.
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 is recalling certain SHERPA NX Active Guiding Catheters used in cardiovascular procedures. The catheters may have a risk of stainless steel wires becoming exposed, which could cause complications during medical procedures.
The catheter's primary segment material could become exposed, revealing underlying stainless steel braid wires. This might cause complications during medical procedures if the wires are inadvertently manipulated.
Healthcare professionals using the catheters for cardiovascular procedures are most at risk. Patients receiving these catheters during procedures may also be affected.
Check for the model 'SHERPA NX ACTIVE GUIDING CATHETER, 6F HSII, .070", REF SA6HSII' with GTIN 00613994824165. All lot and serial numbers are included in the recall.
Verify the model number and GTIN to confirm if your catheter is affected.
Reach out to Medtronic Vascular for specific guidance on next steps.
The recall indicates a potential risk, so it is not recommended for use until further instructions are received.
Check the product details and contact Medtronic Vascular for specific instructions.
Look for the model 'SHERPA NX ACTIVE GUIDING CATHETER, 6F HSII, .070", REF SA6HSII' with GTIN 00613994824165.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2680-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2680-2019 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.
