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Nipro Diagnostics, Inc. recalls MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack.
Recalled February 12, 2014 · FDA recall Z-0910-2014 · Nipro Diagnostics
Hazard
Manufactured with an incorrect factory set unit of measure. · FDA Class II
Units
105
Sold at
Worldwide Distribution - USA (nationwide, HI and Puerto Rico and Internationally to Canada, European Union, Jamaica, Suriname, Trinidad and Tobago, Kazakhastan, Russian, Turkey, Australia, Bangladesh, Pakistan, Cambodia, Laos, Myanmar, Thailand, Vietnam, and India.
Description
Manufactured with an incorrect factory set unit of measure.
Product
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack. Manufactured by: NIPRO 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.
Manufacturer(s)
Nipro Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →