BARD ACCESS SYSTEMS Adverse Event — Injury (MDR MW5005590)
BARD ACCESS SYSTEMS Adverse Event — Injury (MDR MW5005590) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARD ACCESS SYSTEMS; Generic name: GROSHONG; Report number: MW5005590.
| Device | BARD ACCESS SYSTEMS |
|---|---|
| Generic name | GROSHONG |
| Report number | MW5005590 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-19 |
| Narrative | IN 2008 GROSHONG DUAL LUMEN CATHETER IMPLANTED IN UPPER RIGHT CHEST AREA. TWO DAYS LATER, DURING FLUSHING, MEDICAL ASSISTANT NOTICED A LEAK IN ONE OF THE TWO SMALL LINES ENTERING THE BODY. REPEATED EFFORTS TO FLUSH THE BROKEN LINE WERE UNSUCCESSFUL. AND, BECAUSE THE LINE LEAK WAS AT THE ENTRANCE OF THE BODY, IT COULD NOT BE REPAIRED. PIN HOLE. A NEW DUAL LUMEN CATHETER WAS IMPLANTED ABOUT 9 DAYS L |
| Source | openFDA MAUDE (device adverse events) |
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