FDA Adverse Event
Malfunction
Summary report: N
CONTOUR TEST STRIPS
MDR report key: 1854419
·
Received September 29, 2010
Report
- Report Number
- 1826988-2010-00679
- Event Type
- Malfunction
- Date Received
- September 29, 2010
- Date of Event
- September 21, 2010
- Report Date
- September 21, 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
- NJ, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
THE CUSTOMER CALLED FOR HELP WITH HER CONTOUR METER. SHE PERFORMED CONTROL TESTS AND REC'D RESULTS OF 555, 512 AND 286 MG/DL. THE NORMAL CONTROL RANGE WAS 107-148 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 | 7070A | 9JC3B31 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |