AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00370)
AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00370) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AUTO ENDO5 ML; Generic name: CLIP, IMPLANTABLE; Manufacturer: TELEFLEX MEDICAL.
| Device | AUTO ENDO5 ML |
|---|---|
| Generic name | CLIP, IMPLANTABLE |
| Manufacturer | TELEFLEX MEDICAL |
| Report number | 3003898360-2020-00370 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | IT WAS REPORTED THAT THE FIRST CLIP WAS NOT LOADED INTO THE JAWS PROPERLY DURING AN OPERATION. THEN, ACCORDING TO THE USER, THE APPLIER SEEMED TO GET LOCKED. THEREFORE, A NEW UNIT WAS USED INSTEAD. IT IS UNKNOWN WHETHER THE CLIP FELL/REMAINED IN THE PATIENT SO FAR. |
| Source | openFDA MAUDE (device adverse events) |
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