QUATTRODE LEAD, 3/4MM, 60 CM Adverse Event — Injury (MDR 1627487-2020-04262)
QUATTRODE LEAD, 3/4MM, 60 CM Adverse Event — Injury (MDR 1627487-2020-04262) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: QUATTRODE LEAD, 3/4MM, 60 CM; Generic name: QUATTRODE; Manufacturer: ST. JUDE MEDICAL - NEUROMODULATION.
| Device | QUATTRODE LEAD, 3/4MM, 60 CM |
|---|---|
| Generic name | QUATTRODE |
| Manufacturer | ST. JUDE MEDICAL - NEUROMODULATION |
| Report number | 1627487-2020-04262 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | DATE OF THE EVENT IS ESTIMATED. DURING PROCESSING OF THIS COMPLAINT, ATTEMPTS WERE MADE TO OBTAIN COMPLETE PATIENT INFORMATION. THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED. |
| Source | openFDA MAUDE (device adverse events) |
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