FDA Adverse Event
Malfunction
Summary report: N
ACCU-CHEK ® AVIVA COMBO
MDR report key: 3913631
·
Received July 3, 2014
Report
- Report Number
- 1823260-2014-04900
- Event Type
- Malfunction
- Date Received
- July 3, 2014
- Date of Event
- June 6, 2014
- Report Date
- August 4, 2025
- Manufacturer
- ROCHE DIAGNOSTICS
- Product Code
- NBW
- PMA / PMN Number
- NA
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SP
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
- Health Professional
- N
Narratives
Additional Manufacturer Narrative · 1
THE EVENT OCCURRED IN (B)(6). DEVICE WAS NOT REQUESTED TO BE RETURNED.
Description of Event or Problem · 1
PATIENT REPORTED WHEN HE ATTEMPTED TO RUN A BOLUS ADVICE THE METER DID NOT RECOMMEND ANYTHING ALTHOUGH HIS BLOOD GLUCOSE LEVEL WAS 249 MG/DL. PATIENT STATED HE REALIZED THE ADVICE WAS WRONG AND DELIVERED THE CORRESPONDING BOLUS HIMSELF. NO ADVERSE EVENT REPORTED. NO PRODUCT RETURN WAS REQUESTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 391790 | ACCU-CHEK ® AVIVA COMBO | BLOOD GLUCOSE MONITORING DEVICE | NBW | ROCHE DIAGNOSTICS | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 39 YR | Male |