Reported Feb 12, 2014 · Terminated

MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use…

Nipro Diagnostics, 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: Nipro Diagnostics, Inc. · 2400 NW 55th Ct · Ft Lauderdale, FL · 33309-2672

Is this the product you have?

  • MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack
  • Manufactured byNIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A. Is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm
Lot codes and dates
  • Finished GoodsKJ0731
  • Lot Numbers
    • KK0964
    • KL01213
    • KL01233-3TI
    • KL0267-10
    • KL0381-14
    • KL0637-2TI
    • KL0716TI
    • KL0860TI
    • KP0074TI
Amount recalled
105

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

Manufactured with an incorrect factory set unit of measure.

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 Jan 28, 2016 · Data as of Sep 19, 4:52 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.