Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing Recalled by Nipro Diagnostics, Inc. Due to Manufactured with an incorrect factory set unit of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Nipro Diagnostics, Inc. directly.
Affected Products
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.
Quantity: 105
Why Was This Recalled?
Manufactured with an incorrect factory set unit of measure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nipro Diagnostics, Inc.
Nipro Diagnostics, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report