Reported May 25, 2016 · Terminated

Custom Paks containing 23G and 25G valved trocar cannula provide access into the posterior segment of the eye for…

Alcon Research, Ltd.

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: Alcon Research, Ltd. · 6201 South Fwy · Fort Worth, TX · 76134-2099

Is this the product you have?

  • Custom Paks containing 23G and 25G valved trocar cannula provide access into the posterior segment of the eye for surgical instruments within the frame of 23G and 25G Pars-Plana-Vitrectomy (PPV) surgeries.
Lot codes and dates
  • Lot Numbers

    976 of 976 codes

    • 1707828H
    • 1710591H
    • 1710852H
    • 1710853H
    • 1713426H
    • 1713909H
    • 1714519H
    • 1714520H
    • 1715966H
    • 1715967H
    • 1715968H
    • 1715969H
    • 1715973H
    • 1715974H
    • 1715975H
    • 1715978H
    • 1715985H
    • 1715987H
    • 1715990H
    • 1715991H
    • 1715998H
    • 1715999H
    • 1716000H
    • 1716820H
    • 1716821H
    • 1717967H
    • 1718269H
    • 1718273H
    • 1718369H
    • 1718370H
    • 1719092H
    • 1720758H
    • 1720765H
    • 1721380H
    • 1721388H
    • 1721395H
    • 1721590H
    • 1721896H
    • 1722499H
    • 1723082H
    • 1723088H
    • 1723124H
    • 1723841H
    • 1723845H
    • 1723846H
    • 1723876H
    • 1724755H
    • 1724756H
    • 1726782H
    • 1726930H
    • 1726931H
    • 1727056H
    • 1727768H
    • 1729898H
    • 1729997H
    • 1730138H
    • 1730976H
    • 1731351H
    • 1732658H
    • 1732662H
Amount recalled
30,701 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

The product has potential to leak beyond their design specification.

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.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 20, 2017 · Data as of Sep 19, 5:21 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.