DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00293)
DUODOPA_DUOPA Adverse Event — Injury (MDR 3010757606-2020-00293) 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 | 3010757606-2020-00293 |
| 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. (B)(4). THE DEVICE INVOLVED IN THE EVENT WAS NOT RETURNED FOR EVALUATION, IT WAS DISCARDED; THEREFORE, A RETURN SAMPLE EVALUATION WAS NOT PERFORMED. BEZOAR IS A KNOWN COMPLICATION OF A PEG TUBE PLACEMENT. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTA |
| Source | openFDA MAUDE (device adverse events) |
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