DEFIBRILLATOR LEAD Adverse Event — Injury (MDR MW1011548)
DEFIBRILLATOR LEAD Adverse Event — Injury (MDR MW1011548) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DEFIBRILLATOR LEAD; Generic name: DEFIBRILLATOR LEAD; Manufacturer: MEDTRONIC INC..
| Device | DEFIBRILLATOR LEAD |
|---|---|
| Generic name | DEFIBRILLATOR LEAD |
| Manufacturer | MEDTRONIC INC. |
| Report number | MW1011548 |
| Event type | Injury |
| Product problem | Y |
| Date received | 1997-06-24 |
| Narrative | DEFIBRILLATOR LEAD WIRE KNOWN TO BE FRACTURED AND WAS REMOVED AT THE SAME TIME AS ANOTHER FRACTURED LEAD WAS ALSO REMOVED. THE SUBSEQUENT LEAD THAT WAS REMOVED WILL BE REPORTED ON A SEPARATE VOLUNTARY MEDWATCH REPORT. |
| Source | openFDA MAUDE (device adverse events) |
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