OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM Adverse Event — Injury (MDR 1625425-2020-00304)
OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM Adverse Event — Injury (MDR 1625425-2020-00304) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM; Generic name: RETRIEVABLE IVC FILTER; Manufacturer: ARGON MEDICAL DEVICES.
| Device | OPTION RETRIEVABLE VENA CAVA FILTER SYSTEM |
|---|---|
| Generic name | RETRIEVABLE IVC FILTER |
| Manufacturer | ARGON MEDICAL DEVICES |
| Report number | 1625425-2020-00304 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | STUDY, USER FACILITY |
| Narrative | THE SAMPLE DEVICE IS UNAVAILABLE FOR EVALUATION. WITHOUT SUCH EVIDENCE, THE COMPLAINT CANNOT BE CONFIRMED. IF ADDITIONAL INFORMATION IS PROVIDED IN THE FUTURE, THE ISSUE WILL BE RE-EVALUATED AS NEEDED. |
| Source | openFDA MAUDE (device adverse events) |
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