Roche ACCU-CHEK Aviva
Roche · Model ACCU-CHEK Aviva
Quick, 5-second results. Small 0.6 microliter sample size. Contoured, ergonomic design with easy-to-hold rubber grips. 4 customizable test reminders. Downloadable 500-value memory with 7-, 14- and 30-day averaging. Uses 1 readily available 3-volt lithium coin cell battery. 1,000-test battery life. Compatible with ACCU-CHEK data management tools. Preferred on most healthcare plan formularies, so you may save money5.
Typical Failure Modes
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Inaccurate or questionable results
HighSymptoms: Result does not fit the clinical picture, poor duplicate agreement, control solution out of range.
Root cause: Damaged, expired or wrong-lot strips, wrong code chip / key, sample too small, or use outside the operating temperature range.
Meter error / strip problem message
MediumSymptoms: Error code (E-x) during or after a test.
Root cause: Faulty or mis-inserted strip, or a meter fault - repeat with a new strip.
Temperature out-of-range error
MediumSymptoms: Error stating the system is too hot or too cold.
Root cause: Meter and strips outside the specified operating range.
Will not power on / strip not detected
MediumSymptoms: No display on strip insertion, meter will not start a test.
Root cause: Depleted battery or worn / contaminated strip-port contacts.
Serviceable Parts & Consumables
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
Battery
Class Frequent wear itemRel. cost $R&R Easy
Test strips and code chip / key
Class Frequent wear itemRel. cost $R&R Easy
Control solution
Class Frequent wear itemRel. cost $R&R Easy
Strip-port contact assembly
Class Periodic replacementRel. cost $$R&R Moderate
Lancing device
Class Periodic replacementRel. cost $R&R Easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Battery | Frequent wear item | $ | Easy |
| Test strips and code chip / key | Frequent wear item | $ | Easy |
| Control solution | Frequent wear item | $ | Easy |
| Strip-port contact assembly | Periodic replacement | $$ | Moderate |
| Lancing device | Periodic replacement | $ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Troubleshooting Approach
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Result looks wrong
- Repeat with a new strip and an adequate sample.
- Run the control solution and compare to the range on the vial / insert.
- Confirm the code chip / key matches the strip lot.
- Check the ambient temperature is within range.
- If controls fail, quarantine the strip lot; if controls pass but results still look wrong, refer the meter.
Symptom: Error message
- Turn the meter off and repeat with a new strip.
- Move the meter and strips within the operating temperature range.
- Inspect the strip port.
- Replace the battery.
- Contact Roche customer service if it recurs.
Technical Specs
- Height
- 94 mm
- Length
- 22 mm
- Weight
- 60 g
- Width
- 53 mm
Documents & Manuals
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
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.
- RECALL
Inability to dose the test strips, may result in a temporary inability to get a result that could lead to a delay in treatment and/or therapy decisions
- RECALL
The recalling firm identified four US lots of test strips out of specification. Affected strips show increased potential for strip errors prior to applying blood, strips not detected once inserted, or biased results, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result.
- RECALL
Meters may contain a damaged C29 capacitor resulting in issues with power allegation (short battery life or meter not turning on).
- RECALL
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.
- RECALL
Accu-Chek Aviva Nano Blood Glucose meters that were manufactured for the purpose of validating a manufacturing process for product to be distributed outside the US were distributed in the US through eBay by an unauthorized third party. These meters were not intended for distribution, were not verified to meet final product specifications and were not distributed to customers with the necessary pr
- RECALL
Incorrect patient blood glucose test results may be reported due to a software problem.
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