UNK_THROMBECTOMY NEURAVI Adverse Event — Injury (MDR 3011370111-2020-00032)
UNK_THROMBECTOMY NEURAVI Adverse Event — Injury (MDR 3011370111-2020-00032) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNK_THROMBECTOMY NEURAVI; Generic name: CATHETER, THROMBUS RETRIEVER; Manufacturer: NEURAVI LTD..
| Device | UNK_THROMBECTOMY NEURAVI |
|---|---|
| Generic name | CATHETER, THROMBUS RETRIEVER |
| Manufacturer | NEURAVI LTD. |
| Report number | 3011370111-2020-00032 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | FOREIGN, LITERATURE |
| Narrative | PRODUCT COMPLAINT # (B)(4). SINCE THE PRODUCT WAS NOT RETURNED FOR ANALYSIS, NO PRODUCT FAILURE ANALYSIS CAN BE CONDUCTED AND NO DETERMINATION OF POSSIBLE CONTRIBUTING FACTORS COULD BE MADE. DEVICE HISTORY RECORD (DHR) REVIEW CANNOT BE CONDUCTED BECAUSE NO LOT NUMBER WAS PROVIDED BY THE CUSTOMER. MISSING INFORMATION FROM THIS REPORT IS IDENTIFIED AS BLANK; THIS INFORMATION WAS NOT PROVIDED IN THE |
| Source | openFDA MAUDE (device adverse events) |
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