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

Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Aviva Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips, forearm, upper arm, or palm. The Accu-Chek Aviva Plus — recall Z-2766-2019

U.S. FDA — Device Enforcement · United States · 2017-06-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2766-2019
Date of alert: 2017-06-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Roche Diabetes Care, Inc.
Product category: device
Product type: Devices

Reported risk: Meters may contain a damaged C29 capacitor resulting in issues with power allegation (short battery life or meter not turning on).

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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