FOOT CONTROL ASSEMBLY Adverse Event — Injury (MDR 3006524618-2020-00220)
FOOT CONTROL ASSEMBLY Adverse Event — Injury (MDR 3006524618-2020-00220) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FOOT CONTROL ASSEMBLY; Generic name: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES; Manufacturer: ARTHROCARE CORP..
| Device | FOOT CONTROL ASSEMBLY |
|---|---|
| Generic name | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Manufacturer | ARTHROCARE CORP. |
| Report number | 3006524618-2020-00220 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | IT WAS REPORTED THAT DURING THE SURGERY THE FOOT CONTROL WAS NOT WORKING, SURGERY WAS FINISHED USING COMPETITOR DEVICE (BOVIE). NO PATIENT INJURIES OR SIGNIFICANT DELAY REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY. |
| Source | openFDA MAUDE (device adverse events) |
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