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Recall Observatory FDA recall evidence

Device product

ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of the ACCU-CHEK Aviva Combo System)\ The ACCU-CHEK Combo System is indicated for the treatment of insulin-requiring diabetes and for the quantitative measurement of glucose in fresh capillary whole blood from the finger.

Z-0385-2014

October 25, 2013

Class II

Product summary

Firm
Roche Diagnostics Operations, Inc.
Event
Event 66605
Status
Terminated
Classification
Class II
Quantity
6,595 units
Official record key
device-enforcement:Z-0385-2014

Official wording

Reason: There is a software synchronization issue with the ACCU-CHEK Combo system. In rare cases, when the Manual Pump option is chosen on the ACCU-CHEK Aviva Combo meter, there is a possibility of receiving an incorrect bolus advice recommendation that may cause a temporary under delivery of insulin.

Code information: AccuChek Aviva Combo meter 05075645005 packaged in Accu-Chek Combo Kit mg US/English version, 05458544001 and Accu-Chek Combo Kit mg US/Spanish version, 05504686001.

Distribution pattern: Nationwide Distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software synchronization issue