CATHETER Adverse Event — Injury (MDR MW1011546)
CATHETER Adverse Event — Injury (MDR MW1011546) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CATHETER; Generic name: MIDLINE CATHETER; Manufacturer: LUTHER MEDICAL PROD.
| Device | CATHETER |
|---|---|
| Generic name | MIDLINE CATHETER |
| Manufacturer | LUTHER MEDICAL PROD |
| Report number | MW1011546 |
| Event type | Injury |
| Product problem | N |
| Date received | 1997-06-24 |
| Narrative | PT. HAD 20G 20 CM L-CATH BRAND MIDLINE PLACED ON 1-10-97. MOTHER OF PT. TRIPPED OVER CATHETER WHILE PT. PLAYING ON FLOOR. IV CATH WAS PULLED, AND MIDLINE BROKE 1" ABOVE HUB. IV WAS HELD IN PLACE BY STERI STRIPS AND DID NOT FLOAT INTO PT. ER-RN VISIT TO PT, MIDLINE DISCONTINUED AND NEW IV WAS RESTARTED. |
| Source | openFDA MAUDE (device adverse events) |
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