ACCU-CHEK AVIVA TEST STRIPS Adverse Event — Injury (MDR 1823260-2008-01634)
ACCU-CHEK AVIVA TEST STRIPS Adverse Event — Injury (MDR 1823260-2008-01634) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACCU-CHEK AVIVA TEST STRIPS; Generic name: BLOOD GLUCOSE MONITORING TEST STRIPS - LFR; Manufacturer: ROCHE DIAGNOSTICS.
| Device | ACCU-CHEK AVIVA TEST STRIPS |
|---|---|
| Generic name | BLOOD GLUCOSE MONITORING TEST STRIPS - LFR |
| Manufacturer | ROCHE DIAGNOSTICS |
| Report number | 1823260-2008-01634 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-18 |
| Report source | Consumer |
| Narrative | 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 |
| Source | openFDA MAUDE (device adverse events) |
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