Medtronic recalls specific SHERPA NX Active Guiding Catheters for potential wire exposure risk. Affected models include 6F, MP1, 55CM, 070" with serial numbers. Contact for remedy.
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 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's primary segment material can become exposed, revealing stainless-steel braid wires. This may cause complications during procedures if the wires are not properly secured or if the catheter is used incorrectly.
Healthcare professionals using the catheter for cardiovascular procedures are most at risk. Patients receiving these catheters during medical treatments may also be affected.
Check for the model: 6F, MP1, 55CM, 070" with serial number REF SA6MP1K. The catheter is used for cardiovascular procedures and has a GTIN: 00613994821881.
Look for the serial number REF SA6MP1K on the catheter packaging or label.
Reach out to Medtronic Vascular for guidance on next steps and potential remedies.
The recall indicates a potential risk, so it is not recommended for use until further instructions are received from Medtronic.
Contact Medtronic Vascular directly for specific instructions on how to handle the recalled catheter.
Check for the model: 6F, MP1, 55CM, 070" with serial number REF SA6MP1K. The catheter is used for cardiovascular procedures and has a GTIN: 00613994821881.
We’ve drafted a message you can send Medtronic Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-2597-2019 — Medtronic Vascular Medtronic Vascular Hello, I own a Medtronic Vascular that is covered by recall Z-2597-2019 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.
