UNK Adverse Event — Injury (MDR 3005099803-2008-00190)
UNK Adverse Event — Injury (MDR 3005099803-2008-00190) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNK; Generic name: NONE; Manufacturer: BOSTON SCIENTIFIC IRELAND LTD.
| Device | UNK |
|---|---|
| Generic name | NONE |
| Manufacturer | BOSTON SCIENTIFIC IRELAND LTD |
| Report number | 3005099803-2008-00190 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Literature, Company representation |
| Narrative | NOTE: THE EVENT OCCURRED IN 2001 (ACTUAL DATE IS UNK). THE FOLLOWING INFO WAS ASCERTAINED FROM A JOURNAL ARTICLE: STRAINER, L. ET AL (2007) "SELF EXPANDING METALLIC STENTS IN BENIGN POSTOPERATIVE BILIARY STRICTURES: A DIFFICULT SURGICAL OBSTACLE?" HEPATO-GASTROENTEROLOGY. A BOSTON SCIENTIFIC CORPORATION PRODUCT (WALLSTENT BILIARY STENT, MODEL UNK) WAS USED DURING A STENT PLACEMENT PROCEDURE IN A F |
| Source | openFDA MAUDE (device adverse events) |
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