FDA Adverse Event
Malfunction
Summary report: N
ONE TOUCH ULTRALINK METER
MDR report key: 1162392
·
Received September 9, 2008
Report
- Report Number
- 2939301-2008-02105
- Event Type
- Malfunction
- Date Received
- September 9, 2008
- Report Date
- August 21, 2008
- Manufacturer
- LIFESCAN, INC.
- Product Code
- NBW
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- LAY USER/PATIENT
Narratives
Additional Manufacturer Narrative · 1
THE LAY USER/ PATIENT CONTACTED LIFESCAN ALLEGING THAT THE PRODUCT DISPLAY IS DAMAGED AND WAS UNRESOLVED WITH TROUBLESHOOTING. THERE WERE NO ALLEGATIONS OF HARM OR INJURY.
Description of Event or Problem · 1
THE LAY USER/ PATIENT CONTACTED LIFESCAN ALLEGING THAT THE PRODUCT DISPLAY IS DAMAGED AND WAS UNRESOLVED WITH TROUBLESHOOTING. THERE WERE NO ALLEGATIONS OF HARM OR INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ONE TOUCH ULTRALINK METER | GLUCOSE MONITORING SYS/KIT | NBW | LIFESCAN, INC. | NA | 2767028 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |