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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.

DeviceENTERRA GASTRIC STIMULATOR
ManufacturerMEDTRONIC NEUROMODULATION
Report number2182207-2008-00776
Event typeInjury
Product problemN
Date received2008-02-19
Report sourceStudy, Literature, Health Professional
NarrativeJOURNAL 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
SourceopenFDA MAUDE (device adverse events)

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