Abbott Vascular NC Traveler Coronary Catheter Recall: Balloon Deflation Risk

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Recalling firmAbbott Vascular26531 Ynez Rd, D-03Q3, AP52-1 · Temecula, CA 92591-4630

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Abbott Vascular is recalling NC Traveler Coronary Dilatation Catheters (REF 1013157-08) because they may have trouble deflating the balloon. This could lead to complications during medical procedures if the catheter is used improperly.

Why it’s dangerous

The catheter's balloon may not deflate properly during use, which could cause blockages or complications in the blood vessels. This risk is specific to medical procedures where the catheter is used to treat coronary issues.

Who’s affected

Healthcare professionals using this catheter for medical procedures are affected. Patients receiving the catheter as part of their treatment may also be impacted.

How to tell if you have this one

Check for the product name 'NC Traveler Coronary Dilatation Catheter' with part number 1013157-08. The device is not cleared for U.S. distribution and was sold with lot numbers starting with 91010G1.

Brand
Abbott Vascular
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Verify the part number and lot number on the catheter to confirm if it is affected.

✎ GovInfoNow

Questions people ask

Is this catheter safe to use?

The recall states the device is not cleared for U.S. distribution, so it should not be used in the United States.

What should I do if I have this catheter?

The recall does not specify a remedy, so contact Abbott Vascular directly for guidance.

Is there a risk of serious injury?

The hazard description mentions potential balloon deflation issues, but no specific risk of serious injury is stated.

Take action

Contact Abbott Vascular

We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1140-2020 — Abbott Vascular Abbott Vascular

Hello,

I own a Abbott Vascular that is covered by recall Z-1140-2020 from Abbott 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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Where this comes from

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.

Official source: FDA Recall #Z-1140-2020 (January 29, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1140-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Abbott Vascular recalls NC TRAVELER Coronary Dilatation Catheter, REF 1013157-08, Rx Only,NC Traveler RX 4.0 X 8MM The NC Traveler RX Coronary

Lower-risk recall