ABSORB Adverse Event — Death (MDR 2024168-2020-03961)
ABSORB Adverse Event — Death (MDR 2024168-2020-03961) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ABSORB; Generic name: BIORESORBABLE SCAFFOLD; Manufacturer: ABBOTT VASCULAR.
| Device | ABSORB |
|---|---|
| Generic name | BIORESORBABLE SCAFFOLD |
| Manufacturer | ABBOTT VASCULAR |
| Report number | 2024168-2020-03961 |
| Event type | Death |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | LITERATURE |
| Narrative | DATES ESTIMATED. THERE WAS NO REPORTED DEVICE MALFUNCTION AND THE PRODUCT WAS NOT RETURNED. A REVIEW OF THE LOT HISTORY RECORD FOR THE REPORTED LOT COULD NOT BE CONDUCTED BECAUSE THE PART AND LOT NUMBERS WERE NOT PROVIDED. THE REPORTED POTENTIAL ADVERSE EVENTS OF DEATH, MYOCARDIAL INFARCTION AND THROMBOSIS ARE LISTED IN THE ABSORB BIORESORBABLE VASCULAR SCAFFOLD SYSTEM (BVSS), INSTRUCTIONS FOR USE |
| Source | openFDA MAUDE (device adverse events) |
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