KIT CATH MTLUM PRES INJ CVC LF Adverse Event — Injury (MDR MW5094264)
KIT CATH MTLUM PRES INJ CVC LF Adverse Event — Injury (MDR MW5094264) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: KIT CATH MTLUM PRES INJ CVC LF; Generic name: CATHETER, PERCUTANEOUS; Manufacturer: TELEFLEX LLC / / ARROW INTERNATIONAL LLC.
| Device | KIT CATH MTLUM PRES INJ CVC LF |
|---|---|
| Generic name | CATHETER, PERCUTANEOUS |
| Manufacturer | TELEFLEX LLC / / ARROW INTERNATIONAL LLC |
| Report number | MW5094264 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-24 |
| Narrative | PART OF A CENTRAL LINE GUIDE WIRE WAS RETAINED IN THE PATIENT POST CENTRAL LINE PLACEMENT. FDA SAFETY REPORT ID# (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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