Reported Apr 17, 2019 · Terminated

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular…

Vygon U.S.A.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Vygon U.S.A. · 2750 Morris Rd Ste A200 · Lansdale, PA · 19446-6083

Is this the product you have?

  • Vyon DUALSTOP White Cap used
  • for intravascular lines Product Code9888.002-
  • Product UsageCap used for intravascular lines
Lot codes and dates
  • Lot codes090718FD 250118FD 081117FD 130218FD 050418FD 020518FD
Amount recalled
107700

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

DualStop Caps defect causing leaks in affected product

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Vygon U.S.A. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 12, 2020 · Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.