K-WIRE TROCAR, THREADED Adverse Event — Injury (MDR 3012447612-2020-00208)
K-WIRE TROCAR, THREADED Adverse Event — Injury (MDR 3012447612-2020-00208) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: K-WIRE TROCAR, THREADED; Generic name: VITALITY SPINAL FIXATION SYSTEM; Manufacturer: ZIMMER BIOMET SPINE INC..
| Device | K-WIRE TROCAR, THREADED |
|---|---|
| Generic name | VITALITY SPINAL FIXATION SYSTEM |
| Manufacturer | ZIMMER BIOMET SPINE INC. |
| Report number | 3012447612-2020-00208 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | THE PORTION OF THE GUIDE WIRE THAT BROKE OFF AND WAS RETAINED BY THE PATIENT WAS REMOVED ALONG WITH THE IMPLANT CONSTRUCT ON (B)(6) 2020. A PHOTO WAS PROVIDED WHICH SHOWED THE PIECE HAD FRACTURED AS REPORTED AND WAS REMOVED FROM THE PATIENT. IF ADDITIONAL INFORMATION IS OBTAINED THAT ADDS VALUE TO THE RELEVANT CONTENT OF THIS REPORT AND/OR A CONCLUSION CAN BE DRAWN, A FOLLOW-UP REPORT WILL BE SENT |
| Source | openFDA MAUDE (device adverse events) |
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