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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.

DeviceUNK
Generic nameNONE
ManufacturerBOSTON SCIENTIFIC IRELAND LTD
Report number3005099803-2008-00190
Event typeInjury
Product problemY
Date received2008-02-21
Report sourceLiterature, Company representation
NarrativeNOTE: 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
SourceopenFDA MAUDE (device adverse events)

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