COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET Adverse Event — Injury (MDR 3002808486-2020-00446)
COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET Adverse Event — Injury (MDR 3002808486-2020-00446) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET; Generic name: DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR; Ma
| Device | COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET |
|---|---|
| Generic name | DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR |
| Manufacturer | WILLIAM COOK EUROPE |
| Report number | 3002808486-2020-00446 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | PATIENT ALLEGEDLY RECEIVED AN IMPLANT ON (B)(6) 2017 VIA THE RIGHT GROIN DUE TO POST DEEP VEIN THROMBOSIS (DVT). AN (B)(6) 2019 SUCCESSFUL FILTER RETRIEVAL DUE TO DEVICE FAILURE WAS REPORTED. PATIENT IS ALLEGING DEVICE TILT, VENA CAVA PERFORATION COMPLEX REMOVAL, DVT. PATIENT NOTES AND FURTHER ALLEGES EXPERIENCING "DAMAGE TO VEINS, SEVERE CHRONIC SWELLING AND PAIN, LEG DISCOLORATION, MULTIPLE DVT' |
| Source | openFDA MAUDE (device adverse events) |
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