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

Recall Z-0752-2020 — Blood Glucose Monitoring System, Model Number 08313202001 ACCU CHEK GUIDE HCP SAMPLE LAUNCH BOX - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in moni

U.S. FDA — Device Enforcement · United States · 2019-09-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0752-2020
Date of alert: 2019-09-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Roche Diabetes Care, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 08313202001

Reported risk: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring System.

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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