FDA Adverse Event
Malfunction
Summary report: N
ACCU-CHEK COMFORT CURVE TEST STRIPS
MDR report key: 1172569
·
Received September 19, 2008
Report
- Report Number
- 1823260-2008-07031
- Event Type
- Malfunction
- Date Received
- September 19, 2008
- Date of Event
- August 26, 2008
- Report Date
- September 19, 2008
- Manufacturer
- ROCHE DIAGNOSTICS
- Product Code
- LFR
- PMA / PMN Number
- K010362
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- LAY USER/PATIENT
Narratives
Description of Event or Problem · 1
CUSTOMER REPORTED USING 2 DIFFERENT VIALS OF COMFORT CURVE STRIPS FROM THE SAME LOT. REPORTED BLOOD GLUCOSE RESULTS OF 102 MG/DL FROM ONE VIAL AND 189 MG/DL FROM THE SECOND WITHIN 10 MINS ON THE ADVANTAGE SYSTEM. CUSTOMER REPORTED NO SYMPTOMS, DID NOT TREAT OR ACT ON RESULTS. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR THE RETURN OF THE SYSTEM, REPLACEMENT WAS SENT.
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 | 550515 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 49 YR |