DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00296)
DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00296) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DUODOPA_DUOPA; Generic name: TUBES, GASTROINTESTINAL (AND ACCESSORIES); Manufacturer: ABBVIE - MEDICAL DEVICE CENTER.
| Device | DUODOPA_DUOPA |
|---|---|
| Generic name | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
| Manufacturer | ABBVIE - MEDICAL DEVICE CENTER |
| Report number | 3010757606-2020-00296 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL, O |
| Narrative | REFERENCE RECORD (B)(4). CATALOG NUMBER IS THE INTERNATIONAL LIST NUMBER WHICH IS SIMILAR TO US LIST NUMBER OF 062918. THE DEVICE INVOLVED IN THE EVENT REMAINED IMPLANTED IN THE PATIENT; THEREFORE, A RETURN SAMPLE EVALUATION IS UNABLE TO BE PERFORMED. AN ULCER IS A KNOWN COMPLICATION OF A J-TUBE PLACEMENT. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL |
| Source | openFDA MAUDE (device adverse events) |
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