FDA Adverse Event
Malfunction
Summary report: N
ONE TOUCH ULTRA
MDR report key: 702536
·
Received November 14, 2005
Report
- Report Number
- 2939301-2005-04496
- Event Type
- Malfunction
- Date Received
- November 14, 2005
- Report Date
- October 10, 2005
- Manufacturer
- LIFESCAN, INC.
- Product Code
- NBW
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
A PATIENT REPORTED BLOOD GLUCOSE RESULTS OF "124 MG/DL" WITH A LIFESCAN METER AND "163 MG/DLJ" ON A LABORATORY DEVICE, PERFORMED WITHIN 10 MINUTES OF EACH OTHER. THE METER, TEST STRIPS, AND CONTROL SOLUTION WERE REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ONE TOUCH ULTRA | GLUCOSE MONITORING SYS/KIT | NBW | LIFESCAN, INC. | NA | 2568669 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 38 YR |