Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to Meter kit outer boxes containing 10 ct. test...
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
Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determination of glucose in human whole blood taken from finger or forearm. The System is intended to be used to assist the patient and healthcare professional in the management of diabetes.
Quantity: 1,627 Kits
Why Was This Recalled?
Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.
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