GORE TAG THORACIC ENDOPROSTHESIS Adverse Event — Injury (MDR 2017233-2008-00062)
GORE TAG THORACIC ENDOPROSTHESIS Adverse Event — Injury (MDR 2017233-2008-00062) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GORE TAG THORACIC ENDOPROSTHESIS; Generic name: ENDOVASCULAR GRAFT SYSTEM; Manufacturer: W.L. GORE & ASSOCIATES, INC..
| Device | GORE TAG THORACIC ENDOPROSTHESIS |
|---|---|
| Generic name | ENDOVASCULAR GRAFT SYSTEM |
| Manufacturer | W.L. GORE & ASSOCIATES, INC. |
| Report number | 2017233-2008-00062 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Health Professional, Company representation |
| Narrative | A REVIEW OF THE MANUFACTURING PAPERWORK HAS BEEN CONDUCTED. THE REVIEW OF THE MANUFACTURING PAPERWORK VERIFIED THAT THIS LOT MET ALL PRE-RELEASE SPECIFICATIONS. THIS PATIENT WAS ALSO IMPLANT WITH GORE TAG THORACIC ENDOPROSTHESIS (TG3715/LOT# 04400226). |
| Source | openFDA MAUDE (device adverse events) |
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