G7 AUTOMATED HPLC ANALYZER Adverse Event — Malfunction (MDR 2950409-2004-00010)
G7 AUTOMATED HPLC ANALYZER Adverse Event — Malfunction (MDR 2950409-2004-00010) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: G7 AUTOMATED HPLC ANALYZER; Generic name: AUTOMATED HPLC; Manufacturer: TOSOH CORPORATION.
| Device | G7 AUTOMATED HPLC ANALYZER |
|---|---|
| Generic name | AUTOMATED HPLC |
| Manufacturer | TOSOH CORPORATION |
| Report number | 2950409-2004-00010 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2004-10-25 |
| Narrative | CUSTOMER REPORTED THAT G7 AUTOMATED HPLC ANALYZER REPORTED A HA1C RESULT OF 4.2%. RESULT WAS QUESTIONED BY PHYSICIAN; REPEAT RESULT WAS 6.5%. |
| Source | openFDA MAUDE (device adverse events) |
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