FDA Adverse Event
Malfunction
Summary report: N
TRUETRACK
MDR report key: 4251116
·
Received November 5, 2014
Report
- Report Number
- 1052693-2014-00486
- Event Type
- Malfunction
- Date Received
- November 5, 2014
- Date of Event
- October 6, 2014
- Report Date
- December 11, 2015
- Manufacturer
- NIPRO DIAGNOSTICS, INC.
- Product Code
- NBW
- PMA / PMN Number
- K032657
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NH, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
PRODUCT NOT YET RETURNED FOR EVALUATION. (B)(4).
Additional Manufacturer Narrative · 1
(B)(4). INVESTIGATION COMPLETED AND PRODUCT EVALUATED WITH NO DEFECTS FOUND. MOST LIKELY UNDERLYING ROOT CAUSE OF MALFUNCTION:STRIP ISSUE.
Description of Event or Problem · 1
CONSUMER COMPLAINT OF ABOUT BLOOD RESULT READING "LO". LAST 4 RESULTS IN MEMORY WERE "LO", 106MG/DL, 124MG/DL, 115MG/DL. NO ADVERSE EVENT REPORTED.
Description of Event or Problem · 1
CONSUMER COMPLAINT OF ABOUT BLOOD RESULT READING "LO". LAST 4 RESULTS IN MEMORY WERE "LO", 106MG/DL, 124MG/DL, 115MG/DL. NO ADVERSE EVENT REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 710159 | TRUETRACK | BLOOD GLUCOSE SYSTEM | NBW | NIPRO DIAGNOSTICS, INC. | TRUETRACK | RR4463 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 0 YR |