Reported Jul 1, 2015 · Terminated

VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…

Remel Inc.

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: Remel Inc · 12076 Santa Fe Trail Dr · Lenexa, KS · 66215-3519

Is this the product you have?

  • VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
Lot codes and dates
  • Serial numbers

    143 of 143 codes

    • 0169039201140624
    • 0169040501140626
    • 0169050101141007
    • 0169068601141216
    • 0169078101150213
    • 2163X1013
    • 2164X1013
    • 2165X1013
    • 2166X1013
    • 2167X1013
    • 2168X1013
    • 2169X1013
    • 2170X1013
    • 2171X1013
    • 2172X1013
    • 2173X1013
    • 2174X1013
    • 2175X1013
    • 2176X1013
    • 2177X1013
    • 2178X1013
    • 2179X1013
    • 2180X1013
    • 2181X1013
    • 2182X1013
    • 2183X1013
    • 2184X1013
    • 2185X1013
    • 2186X1013
    • 2187X1013
    • 2188X1013
    • 2189X1013
    • 2190X1013
    • 2191X1013
    • 2192X1113
    • 2193X1113
    • 2194X1113
    • 2195X1113
    • 2196X1113
    • 2199X1113
    • 2201X1113
    • 2202X1113
    • 2203X1113
    • 2204X1113
    • 2205X1113
    • 2206X1113
    • 2207X1113
    • 2208X1113
    • 2209X1113
    • 2210X1113
    • 2211X1113
    • 2212X1113
    • 2213X1113
    • 2214X1113
    • 2216X1113
    • 2217X1113
    • 2218X1213
    • 2219X1213
    • 2220X1213
    • 2221X1213
Amount recalled
143 devices

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

Why it was recalled

Use of the recalled product may result in false positive reports.

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

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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 Mar 24, 2017 · Data as of Sep 19, 6:07 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.