PRECISION XTRA/OPTIUM Adverse Event — Malfunction (MDR 2954323-2008-00809)
PRECISION XTRA/OPTIUM Adverse Event — Malfunction (MDR 2954323-2008-00809) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION XTRA/OPTIUM; Generic name: BLOOD GLUCOSE METER; Manufacturer: ABBOTT DIABETES CARE LIMITED UK.
| Device | PRECISION XTRA/OPTIUM |
|---|---|
| Generic name | BLOOD GLUCOSE METER |
| Manufacturer | ABBOTT DIABETES CARE LIMITED UK |
| Report number | 2954323-2008-00809 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Consumer |
| Narrative | A CUSTOMER REPORTED AN ISSUE WITH THE DISPLAY ON THEIR PRECISION XTRA BLOOD GLUCOSE METER. UPON PRODUCT INVESTIGATION, IT WAS DISCOVERED THE METER EXHIBITED A DISPLAY ISSUE. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY OR MISTREATMENT ASSOCIATED WITH THIS EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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