Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB SH, .070" REF SA6RCBSH for cardiovascular use due to potential loss of primary segment material exposing stainless-steel wires.
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 because it may expose underlying steel wires, which could cause serious injury during use. This recall affects medical devices used in procedures like angioplasty or stent placement.
The catheter's primary segment material can break off, exposing the stainless-steel braid wires. This could lead to complications like tissue damage or blockages during medical procedures.
Healthcare professionals using the specific catheter model for cardiovascular procedures are most at risk. Patients undergoing procedures with this catheter may also be affected.
Check for the model name 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F RCB SH, diameter .070", and reference number SA6RCBSH. The product was sold with GTIN 00613994823274.
Verify the model, size, and reference number to confirm if your catheter is affected.
The recall states there is a potential for wire exposure, so it is not safe to use without the remedy.
Check for the model 'SHERPA NX ACTIVE GUIDING CATHETER', size 6F RCB SH, diameter .070", and reference number SA6RCBSH.
The recall 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-2685-2019 — 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-2685-2019 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.
