PRECISION XTRA Adverse Event — Malfunction (MDR 2954323-2020-02938)
PRECISION XTRA Adverse Event — Malfunction (MDR 2954323-2020-02938) 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 | 2954323-2020-02938 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | TO DATE, PRODUCT HAS NOT BEEN RETURNED FOR FURTHER INVESTIGATION. PRECISION XTRA METERS ARE GUARANTEED TO BE FREE FROM DEFECTS IN MATERIAL AND WORKMANSHIP FOR A PERIOD OF NO MORE THAN 4 YEARS FROM THE DATE OF PURCHASE. AS THE MANUFACTURING DATE OF THIS PRODUCT IS BEFORE 2010, IT HAS BEEN IN DISTRIBUTION BEYOND ITS USEFUL LIFE AT THE TIME OF THE COMPLAINT. SINCE THE PRODUCT EXCEEDED ITS USEFUL LIFE |
| Source | openFDA MAUDE (device adverse events) |
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