Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1140-2013 — 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 profession

U.S. FDA — Device Enforcement · United States · 2013-02-25 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1140-2013
Date of alert: 2013-02-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Nipro Diagnostics, Inc.
Product category: device
Product type: Devices

Reported risk: Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related