AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00374)
AUTO ENDO5 ML Adverse Event — Malfunction (MDR 3003898360-2020-00374) 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 | 3003898360-2020-00374 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | (B)(4). THE DEVICE HISTORY REVIEW FOR THE PRODUCT AUTO ENDO5 ML LOT 73G1900045 INVESTIGATION DID NOT SHOW ISSUES RELATED TO THE COMPLAINT. THE DEVICE HAS NOT BEEN RETURNED FOR INVESTIGATION. TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS. |
| Source | openFDA MAUDE (device adverse events) |
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