FREESTYLE FLASH Adverse Event — Injury (MDR 2954323-2008-00824)
FREESTYLE FLASH Adverse Event — Injury (MDR 2954323-2008-00824) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FREESTYLE FLASH; Generic name: BLOOD GLUCOSE MONITORING SYSTEM; Manufacturer: ABBOTT DIABETES CARE INC, USA.
| Device | FREESTYLE FLASH |
|---|---|
| Generic name | BLOOD GLUCOSE MONITORING SYSTEM |
| Manufacturer | ABBOTT DIABETES CARE INC, USA |
| Report number | 2954323-2008-00824 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Consumer |
| Narrative | CUSTOMER'S MOTHER REPORTED NOT BEING ABLE TO TEST CUSTOMER'S BLOOD GLUCOSE DUE TO BLANK SCREEN THAT APPEARS ON THEIR FREESTYLE FLASH METER. AS A RESULT, THE CUSTOMER WENT TO CONSULT THEIR DOCTOR. CUSTOMER'S MOTHER REPORTED CUSTOMER EXPERIENCED SYMPTOMS OF "UPPER BODY SHAKINESS, LEFT HAND TREMBLES, FATIGUE AND DIABETIC SEIZURE" DURING THEIR DOCTOR'S APPOINTMENT. CUSTOMER'S MOTHER REPORTED CUSTOMER |
| Source | openFDA MAUDE (device adverse events) |
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