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

Recall Z-0910-2014 — 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

U.S. FDA — Device Enforcement · United States · 2013-10-02 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0910-2014
Date of alert: 2013-10-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Nipro Diagnostics, Inc.
Product category: device
Product type: Devices

Reported risk: Manufactured with an incorrect factory set unit of measure.

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.

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