DLP-W11 Adverse Event — Other (MDR 1718873-2008-00001)
DLP-W11 Adverse Event — Other (MDR 1718873-2008-00001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DLP-W11; Generic name: LOOP ELECTRODE; Manufacturer: UTAH MEDICAL PRODUCTS, INC..
| Device | DLP-W11 |
|---|---|
| Generic name | LOOP ELECTRODE |
| Manufacturer | UTAH MEDICAL PRODUCTS, INC. |
| Report number | 1718873-2008-00001 |
| Event type | Other |
| Product problem | * |
| Date received | 2008-01-24 |
| Report source | Other, Health Professional |
| Narrative | EVENT WAS REPORTED BY THE MEDICAL FACILITY AS A PROD PROBLEM. NOT AN ADVERSE EVENT. PROCEDURE WAS COMPLICATED BY HEMORRHAGE AND COLLATERAL TISSUE DAMAGE. THE CAUSE OF THE COLLATERAL DAMAGE COULD NOT BE DETERMINED BY THE MEDICAL PRACTITIONERS. IN THE ABSENCE OF A TRAINED CLINICIAN INDICATION OF RISK OF SERIOUS INJURY, UTMD IS UNABLE TO DETERMINE THE LIKELY HOOD OF SERIOUS INJURY. IF THE EVENT WERE |
| Source | openFDA MAUDE (device adverse events) |
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