PRECISION XTRA/OPTIUM Adverse Event — Injury (MDR 2954323-2008-00748)
PRECISION XTRA/OPTIUM Adverse Event — Injury (MDR 2954323-2008-00748) 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 | 2954323-2008-00748 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-07 |
| Report source | Consumer |
| Narrative | THE PRODUCT WAS RETURNED AND INVESTIGATED, AND THE COMPLAINT WAS NOT CONFIRMED. NO NEW ISSUES WERE OBSERVED. ALL RESULTS WERE WITHIN RANGE SPECIFICATION, AND NO ERRORS WERE OBSERVED DURING CONTROL SOLUTION TESTING. |
| Source | openFDA MAUDE (device adverse events) |
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