GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET Adverse Event — Injury (MDR 3002808486-2020-00450)
GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET Adverse Event — Injury (MDR 3002808486-2020-00450) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET; Generic name: DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR; Manufacturer: WILL
| Device | GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET |
|---|---|
| Generic name | DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR |
| Manufacturer | WILLIAM COOK EUROPE |
| Report number | 3002808486-2020-00450 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | PATIENT ALLEGEDLY RECEIVED AN IMPLANT ON (B)(6)2015 VIA THE RIGHT INTERNAL JUGULAR VEIN DUE TO DEEP VEIN THROMBOSIS. THE PLAINTIFF ALLEGES VENA CAVA PERFORATION. THE PLAINTIFF FURTHER ALLEGES EMOTIONAL DISORDER. (B)(6)2018 , PER A REPORT FROM COMPUTED TOMOGRAPHY; ¿POSITIVE FOR CAVAL PERFORATION. SUPERIOR EXTENT OF IVC FILTER MID L2 VERTEBRAL BODY. INFERIOR EXTENT L3-L4 DISC. A TOTAL OF 4 PRONGS HA |
| Source | openFDA MAUDE (device adverse events) |
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