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

Recall Z-3201-2018 — Contour Plus Link 2.4, Product Catalog Number: MMT-1151SK. wireless blood glucose monitoring system Contour Plus LINK 2.4 wireless blood glucose monitoring system (glucometer, test strips and control solution) is designed for self-testing by persons with diabetes and the monitoring of glucose co

U.S. FDA — Device Enforcement · United States · 2018-05-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3201-2018
Date of alert: 2018-05-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medtronic Inc.
Product category: device
Product type: Devices

Reported risk: CONTOUR PLUS LINK 2.4 meter with an incorrect unit of measure was included into meter kits and distributed. This meter contains the incorrect unit of measure mg/dL instead of mmol/L.

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

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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.

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