HUMAPEN, UNKNOWN DEVICE Adverse Event — Injury (MDR 1819470-2020-00042)
HUMAPEN, UNKNOWN DEVICE Adverse Event — Injury (MDR 1819470-2020-00042) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HUMAPEN, UNKNOWN DEVICE; Generic name: FOR TREATMENT PURPOSES; Manufacturer: ELI LILLY AND COMPANY.
| Device | HUMAPEN, UNKNOWN DEVICE |
|---|---|
| Generic name | FOR TREATMENT PURPOSES |
| Manufacturer | ELI LILLY AND COMPANY |
| Report number | 1819470-2020-00042 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | NARRATIVE FIELD: NEW, UPDATED AND CORRECTED INFORMATION IS REFERENCED WITHIN THE UPDATE STATEMENTS. PLEASE REFER TO UPDATE STATEMENT(S) DATED 04MAY2020. NO FURTHER FOLLOW-UP IS PLANNED. EVALUATION SUMMARY: A MALE PATIENT REPORTED THAT THE SCALE ON THE DOSE WINDOW OF HIS HUMAPEN (UNKNOWN DEVICE TYPE) DEVICE WAS CLOUDY. THE PATIENT EXPERIENCED ABNORMAL BLOOD GLUCOSE. THE DEVICE WAS NOT RETURNED TO T |
| Source | openFDA MAUDE (device adverse events) |
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