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

Recall Z-0413-2026 — Good Neighbor Pharmacy, TRUE METRIX Self Monitoring Blood Glucose Meter. Model/Catalog Number: RE4011-01.

U.S. FDA — Device Enforcement · United States · 2025-10-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0413-2026
Date of alert
2025-10-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Trividia Health, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00087701426254
Reported risk: Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management.
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.

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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.