FDA Adverse Event
Malfunction
Summary report: N
ONE TOUCH ULTRA
MDR report key: 653572
·
Received December 12, 2005
Report
- Report Number
- 2939301-2005-05611
- Event Type
- Malfunction
- Date Received
- December 12, 2005
- Report Date
- December 8, 2005
- Manufacturer
- LIFESCAN, INC.
- Product Code
- NBW
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
THE PATIENT REPORTED BLOOD GLUCOSE RESULTS OF 195, 182, 191, AND 280 MG/DL"WITH THE LIFESCAN METER, PERFORMED WITHIN 10 MINUTES OF EACH OTHER. THE CONTROL SOLUTION WAS REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ONE TOUCH ULTRA | GLUCOSE MONITORING SYS/KIT | NBW | LIFESCAN, INC. | NA | 2535461 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |