Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if you own this device for cardiovascular 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 internal wires becoming exposed. This could lead to complications during medical procedures if the catheter is used improperly.
The catheter may lose its outer protective layer, exposing the internal stainless-steel wires. This could cause tissue damage or other complications during medical procedures if the catheter is used without proper protection.
Patients undergoing cardiovascular procedures who use the recalled catheter model are affected. Medical professionals using the device for procedures are at higher risk due to the potential for complications.
Check for the model name SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC3.75, .070", REF SA6MAC375. The device is used for cardiovascular procedures and has a specific GTIN number.
Identify the model number on the catheter to confirm if it matches the recalled SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC3.75, .070", REF SA6MAC375.
The recall indicates a potential risk, but the catheter is generally safe for use. Patients should follow the manufacturer's instructions and contact Medtronic Vascular if they have the recalled model.
The recall does not specify a remedy, so you should check with Medtronic Vascular to confirm if your device is affected and follow their guidance.
Look for the model name SHERPA NX ACTIVE GUIDING CATHETER, 6F MAC3.75, .070", REF SA6MAC375. on the device or its packaging.
We’ve drafted a message you can send Medtr: Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2687-2019 — Medtr: Vascular Medtr: Vascular Hello, I own a Medtr: Vascular that is covered by recall Z-2687-2019 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.
