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

Recall Z-2351-2021 — Accu-Chek Aviva Plus Test Strip, Blood Glucose Monitoring System, Model numbers: 06908152001, 06908217001, 06908268001, 06908349001, 06908373001

U.S. FDA — Device Enforcement · United States · 2021-07-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2351-2021
Date of alert
2021-07-28
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)
06908152001
Reported risk: Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.
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.