ACCU-CHEK AVIVA TEST STRIPS
Report
- Report Number
- 1823260-2008-01634
- Event Type
- Injury
- Date Received
- February 18, 2008
- Date of Event
- January 25, 2008
- Report Date
- February 18, 2008
- Manufacturer
- ROCHE DIAGNOSTICS
- Product Code
- LFR
- PMA / PMN Number
- K043474
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- LAY USER/PATIENT
Narratives
THIS MEDWATCH REPORT IS FOR THE SUSPECT DEVICE USED IN SYSTEM 1 (LOT NUMBER 300971, EXPIRATION DATE 05/31/2009). REFERENCE MEDWATCH REPORT WITH PATIENT FOR THE SUSPECT DEVICE USED IN SYSTEM 2.
REPORTER ALLEGED OBTAINING A BLOOD GLUCOSE RESULT OF 200 MG/DL ON THE AVIVA SYSTEM 1 AND THEN TAKING AN EXTRA 50 MG OF JANUVIA IN ADDITION TO THE 50 MG SHE NORMALLY TAKES. REPORTER STATED THAT 15 MINS LATER, SHE BEGAN FEELING HYPOGLYCEMIC SYMPTOMS. REPORTER INDICATED THAT HER FAMILY ATTEMPTED TO TREAT HER WITH SUGAR BUT SHE WAS UNABLE TO EAT IT, SO THEY CALLED THE EMTS AND ATTEMPTED TO TEST HER ON AVIVA SYSTEM 2, BUT IT WOULD NOT TURN ON DUE TO POWER CONCERNS. REPORTER STATED THAT THE EMTS TOOK HER TO THE HOSP WHERE A LOW RESULT WAS OBTAINED, SHE RECEIVED AN IV, WAS GIVEN A SANDWICH AND THEN RELEASED WITHIN 4 HRS. NO OTHER ACTIONS WERE REPORTED TAKEN OR TREATMENT RECEIVED. A REQUEST WAS MADE FOR THE RETURN OF THE SUSPECT DEVICE AND REPLACEMENT PRODUCT WAS SENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACCU-CHEK AVIVA TEST STRIPS | BLOOD GLUCOSE MONITORING TEST STRIPS - LFR | LFR | ROCHE DIAGNOSTICS | 300971 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 46 YR | Hospitalization| R | JANUVIA - 2 YRS 50 MG DAILY| ACCUPRIL - 7 YRS 80 MG DAILY| STARLIX - 7 YRS - 60 MG DAILY| DILTIAZEM - 7 YRS 240 MG DAILY| HYDROCHLOROTHIAZIDE - 7 YRS 25 MG DAILY| PLAVIX - 7 YRS 75 MG DAILY| METFORMIN - 7 YRS - 2000 MG DAILY| BYETTA - 1 YR - 1 SHOT DAILY |