LUGE Adverse Event — Injury (MDR 2134265-2008-00452)
LUGE Adverse Event — Injury (MDR 2134265-2008-00452) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LUGE; Generic name: DQX WIRE, GUIDE, CATHETER; Manufacturer: BOSTON SCIENTIFIC.
| Device | LUGE |
|---|---|
| Generic name | DQX WIRE, GUIDE, CATHETER |
| Manufacturer | BOSTON SCIENTIFIC |
| Report number | 2134265-2008-00452 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Health Professional, Company representation |
| Narrative | SAME CASE AS MFR REPORT# 2134265-2008-00453. SAME CASE AS MFR REPORT# 2134265-2008-00454. SAME CASE AS MFR REPORT# 2134265-2008-00455. IT WAS REPORTED THAT DURING AN UNSPECIFIED PROCEDURE, A GUIDE WIRE SEPARATION OCCURRED. THE LESION WAS LOCATED IN THE LEFT ANTERIOR DESCENDING (LAD) ARTERY. THE PERCENT OF THE STENOSIS, DEGREE OF CALCIFICATION, AND VESSEL TORTUOUSITY ARE UNK. A 300CM LUGE GUIDE WIR |
| Source | openFDA MAUDE (device adverse events) |
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