Medtronic recalls specific SHERPA NX Active Guiding Catheters for 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 is recalling certain SHERPA NX Active Guiding Catheters used in cardiovascular procedures. The catheters may have exposed stainless steel wires that could cause injury if used improperly.
The catheter may lose its primary segment material, exposing the underlying stainless steel braid wires. This could lead to injury if the wires are accidentally cut or snagged during procedures.
Cardiovascular professionals who use the recalled catheters for procedures are most at risk. Patients undergoing procedures with these catheters could face injury if the wires are exposed.
Check for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, RDC, 55CM, 070", REF SA6RDCK. The product was sold with GTIN 00613994823250 and all lot/serial numbers.
Review the model number and GTIN to confirm if your catheter is affected.
The recall states there is a potential for wire exposure, so affected units should not be used until the remedy is applied.
Check for the model: SHERPA NX ACTIVE GUIDING CATHETER, 6F, RDC, 55CM, 070", REF SA6RDCK. The product was sold with GTIN 00613994823250 and all lot/serial numbers.
The recall does not specify a remedy, so contact Medtronic Vascular directly for guidance.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2606-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2606-2019 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.
