FDA Adverse Event
Malfunction
Summary report: N
ACCU-CHEK COMFORT CURVE TEST STRIPS
MDR report key: 1190584
·
Received October 6, 2008
Report
- Report Number
- 1823260-2008-07369
- Event Type
- Malfunction
- Date Received
- October 6, 2008
- Date of Event
- September 28, 2008
- Report Date
- October 6, 2008
- Manufacturer
- ROCHE DIAGNOSTICS
- Product Code
- LFR
- PMA / PMN Number
- K010362
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- LAY USER/PATIENT
Narratives
Description of Event or Problem · 1
THE CUSTOMER STATES THAT SHE OBTAINED THE FOLLOWING BLOOD GLUCOSE COMPARISONS ON THE ACCU-CHEK ADVANTAGE SYSTEM (PER METER MEMORY): 308MG/DL AND 130MG/DL; 160MG/DL AND 88MG/DL. THE AFOREMENTIONED TESTS WERE OBTAINED WITHIN 10 MINUTES. NO REPORTED ACTIONS TAKEN OR TREATMENT RENDERED. NO ADVERSE EVENT REPORTED. NEW SYSTEM SENT TO CUSTOMER AND RETURN REQUESTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACCU-CHEK COMFORT CURVE TEST STRIPS | BLOOD GLUCOSE MONITORING TEST STRIPS - LFR | LFR | ROCHE DIAGNOSTICS | 550510 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR | "REGULIN"| NOVOLOG| LISINOPRIL| PRILOSEC| LANTUS| ZETIA |