FDA Adverse Event
Malfunction
Summary report: N
CONTOUR TEST STRIPS
MDR report key: 1884659
·
Received October 25, 2010
Report
- Report Number
- 1826988-2010-00714
- Event Type
- Malfunction
- Date Received
- October 25, 2010
- Date of Event
- October 7, 2010
- Report Date
- October 7, 2010
- Manufacturer
- BAYER HEALTHCARE LLC
- Product Code
- NBW
- PMA / PMN Number
- K062058
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
THE ADVOCATE CALLED FOR HELP WITH THE CUSTOMER'S CONTOUR METER. WHILE TROUBLESHOOTING, HE PERFORMED CONTROL TESTS AND REC'D A RESULT OF 16 MG/DL. THE NORMAL CONTROL RANGE WAS 105-146 MG/DL. NO ADVERSE EVENTS WERE ALLEGED. THE TEST STRIPS ARE TO BE RETURNED FOR EVAL. REPLACEMENT TEST STRIPS AND A NEW METER WERE SENT TO THE CUSTOMER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CONTOUR TEST STRIPS | NBW | BAYER HEALTHCARE LLC | 7097C | 9GC3C10 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |