Vygon DualStop White Cap Recall: Leaks Risk in Intravascular Lines

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Recalling firmVygon U.S.A.2750 Morris Rd Ste A200, N/A · Lansdale, PA 19446-6083

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Vygon is recalling DualStop White Caps used for intravascular lines because they can leak. This defect could lead to complications if the caps fail during medical procedures.

Why it’s dangerous

The DualStop White Caps can leak due to a defect, which might cause issues during medical procedures. Leaks could lead to complications if the caps fail while in use.

Who’s affected

Healthcare professionals using these caps for intravascular lines are most at risk. Patients receiving treatments with these caps may also be affected.

How to tell if you have this one

Check for product codes: 090718FD, 250118FD, 081117FD, 130218FD, 050418FD, or 020518FD. These caps are used for intravascular lines in medical settings.

Brand
Vygon
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Code
Look for the product codes listed: 090718FD, 250118FD, 081117FD, 130218FD, 050418FD, or 020518FD.

✎ GovInfoNow

Questions people ask

What is the defect in the DualStop White Caps?

The DualStop White Caps can leak due to a defect.

How can I tell if I have the recalled product?

Check for product codes: 090718FD, 250118FD, 081117FD, 130218FD, 050418FD, or 020518FD.

Do I need to stop using the caps immediately?

The recall does not specify an immediate stop; check the product code first.

Take action

Contact Vygon

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

✉️ Open in email

Subject: Recall Z-1115-2019 — Vygon Vygon

Hello,

I own a Vygon that is covered by recall Z-1115-2019 from Vygon.

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-1115-2019 (December 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1115-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.

Vygon U.S.A. recalls Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular

Lower-risk recall