ZENITH RENU CONVERTER AAA ANCILLARY GRAFT Adverse Event — Injury (MDR 1820334-2008-00107)
ZENITH RENU CONVERTER AAA ANCILLARY GRAFT Adverse Event — Injury (MDR 1820334-2008-00107) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ZENITH RENU CONVERTER AAA ANCILLARY GRAFT; Generic name: MIH ENDOVASCULAR GRAFT; Manufacturer: COOK INCORPORATED.
| Device | ZENITH RENU CONVERTER AAA ANCILLARY GRAFT |
|---|---|
| Generic name | MIH ENDOVASCULAR GRAFT |
| Manufacturer | COOK INCORPORATED |
| Report number | 1820334-2008-00107 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-21 |
| Report source | Health Professional, Company representation |
| Narrative | A MALE HAD A RENU CUFF PLACED ON AN UNKNOWN DATE. A CORE LAB INTERPRETATION OF THE 3-MONTH AND 6-MONTH CT SCANS INDICATED A FOCAL LEFT DISTAL TYPE I ENDOLEAK DUE TO THE RENU CUFF. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. |
| Source | openFDA MAUDE (device adverse events) |
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