MEDTRONIC Adverse Event — Injury (MDR MW5005538)
MEDTRONIC Adverse Event — Injury (MDR MW5005538) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDTRONIC; Generic name: SENSIA S.R. PACEMAKER; Manufacturer: MEDTRONIC INC..
| Device | MEDTRONIC |
|---|---|
| Generic name | SENSIA S.R. PACEMAKER |
| Manufacturer | MEDTRONIC INC. |
| Report number | MW5005538 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-18 |
| Narrative | HAVE IRREGULAR HEART RHYTHMS - HAD PACER REPLACED DUE TO LOW BATTERY, STILL HAVING SYMPTOMS WHICH DATE BACK TO 2000. I RECENTLY HAD PACEMAKER REPLACED, DUE TO LOW BATTERY, AND IRREGULAR HEART RHYTHMS BY DR. HE MENTIONED THE PACER LED TO THE HEART COULD BE FRACTURED OR CRACKED AND WAS CONCERNED, BUT LOOKED LIKE OK CONDITION WHEN PROCEDURE WAS DONE. I SAW ON TV COMMERICAL, THEIR COMMERCIAL MEDTRONIC |
| Source | openFDA MAUDE (device adverse events) |
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