AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00371)
AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00371) 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 | 3003898360-2020-00371 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | (B)(4). THE DEVICE HISTORY REVIEW FOR THE PRODUCT AUTO ENDO5 ML LOT# 73E1900345 INVESTIGATION DID NOT SHOW ISSUES RELATED TO COMPLAINT. THE DEVICE INVESTIGATION IS PENDING. TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS. |
| Source | openFDA MAUDE (device adverse events) |
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