DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00294)
DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00294) 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 | 3010757606-2020-00294 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER, FOREIGN, HEALTH PROFE |
| Narrative | REFERENCE RECORD (B)(4). CATALOG NUMBER IS THE INTERNATIONAL LIST NUMBER WHICH IS SIMILAR TO US LIST NUMBER OF 062910. THE DEVICE INVOLVED IN THE EVENT REMAINED IMPLANTED IN THE PATIENT AND WAS NOT RETURNED; THEREFORE, A RETURN SAMPLE EVALUATION IS UNABLE TO BE PERFORMED. STOMA SITE INFECTION IS A KNOWN COMPLICATION OF A PEG TUBE PLACEMENT. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTA |
| Source | openFDA MAUDE (device adverse events) |
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