CENTURION Adverse Event — Report (MDR 10000305)
CENTURION Adverse Event — Report (MDR 10000305) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CENTURION; Generic name: CARDIAC CATHETERIZATION KIT; Manufacturer: CENTURION MEDICAL PRODUCTS CORPORATION.
| Device | CENTURION |
|---|---|
| Generic name | CARDIAC CATHETERIZATION KIT |
| Manufacturer | CENTURION MEDICAL PRODUCTS CORPORATION |
| Report number | 10000305 |
| Product problem | N |
| Date received | 2020-04-27 |
| Narrative | CENTURION INTRO-FLEX 8.5F SINGLE LUMEN, LOT# 2020020750, EXP 12/31/2020, ECVC6325. DURING PLACEMENT TO RIGHT INTERNAL JUGULAR (IJ), WHILE TRYING TO REMOVE GUIDEWIRE, GUIDEWIRE WAS KINKED, MAKING REMOVAL DIFFICULT. LINE WAS ABLE TO BE SAVED, PATIENT WAS NOT RE-STUCK. GUIDEWIRE AND PACKING PROVIDED FOR REVIEW. LOCATION: EMERGENCY DEPARTMENT. |
| Source | openFDA MAUDE (device adverse events) |
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