ENTERRA GASTRIC STIMULATOR Adverse Event — Injury (MDR 2182207-2008-00776)
ENTERRA GASTRIC STIMULATOR Adverse Event — Injury (MDR 2182207-2008-00776) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENTERRA GASTRIC STIMULATOR; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00776.
| Device | ENTERRA GASTRIC STIMULATOR |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00776 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Study, Literature, Health Professional |
| Narrative | JOURNAL REF: LIU ET AL. "EROSION OF GASTRIC ELECTRICAL STIMULATOR ELECTRODES: EVAL, MANAGEMENTS, AND LAPAROSCOPIC TECHNIQUES." SURG LAPAROSC ENDOSC PERCUTAN TECH 2007; 17(5): 438-441. THIS ARTICLE DESCRIBES TWO CASE REPORTS OF PTS WITH DIABETIC GASTROPARESIS THAT WERE TREATED WITH GASTRIC STIMULATION AND HAD ELECTRODE EROSION. A FEMALE WITH DIABETIC GASTROPARESIS UNDERWENT LAPAROSCOPIC PLACEMENT O |
| Source | openFDA MAUDE (device adverse events) |
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