FDA Adverse Event
Malfunction
Summary report: N
CONTOUR
MDR report key: 3090419
·
Received May 2, 2013
Report
- Report Number
- 1826988-2013-00184
- Event Type
- Malfunction
- Date Received
- May 2, 2013
- Date of Event
- April 1, 2013
- Report Date
- April 8, 2013
- Manufacturer
- BAYER HEALTHCARE LLC
- Product Code
- NBW
- PMA / PMN Number
- K062058
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE CUSTOMER RECEIVED A BLOOD GLUCOSE READING OF 135MG/DL ON THE CONTOUR METER, RE-TESTED ON THE CONTOUR USB METER AND THE READING WAS 348MG/DL. THE DIFFERENCE BETWEEN THE READINGS FALLS IN THE "C" ZONE OF THE CONSENSUS ERROR GRID, MAKING THE DIFFERENCE CLINICALLY SIGNIFICANT NO ADVERSE EVENT WAS ALLEGED. THE TEST STRIPS ARE NOT AVAILABLE TO RETURN FOR EVALUATION. A NEW METER WAS SENT TO THE CUSTOMER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 192434 | CONTOUR | BLOOD GLUCOSE METER | NBW | BAYER HEALTHCARE LLC | 9556C |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |