PRECISION XTRA Adverse Event — Malfunction (MDR 2954323-2020-02956)
PRECISION XTRA Adverse Event — Malfunction (MDR 2954323-2020-02956) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION XTRA; Generic name: BLOOD GLUCOSE MONITORING SYSTEM; Manufacturer: ABBOTT DIABETES CARE INC.
| Device | PRECISION XTRA |
|---|---|
| Generic name | BLOOD GLUCOSE MONITORING SYSTEM |
| Manufacturer | ABBOTT DIABETES CARE INC |
| Report number | 2954323-2020-02956 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | UNLESS FURTHER INFORMATION IS OBTAINED, THIS ISSUE IS CONSIDERED CLOSED. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT DIABETES CARE HAS BEEN SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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