PRLNE HERNIA SYSTEM MSH 10CM UNDERLAY Adverse Event — Injury (MDR 2210968-2020-03491)
PRLNE HERNIA SYSTEM MSH 10CM UNDERLAY Adverse Event — Injury (MDR 2210968-2020-03491) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRLNE HERNIA SYSTEM MSH 10CM UNDERLAY; Generic name: MESH, SURGICAL, POLYMERIC; Manufacturer: ETHICON INC..
| Device | PRLNE HERNIA SYSTEM MSH 10CM UNDERLAY |
|---|---|
| Generic name | MESH, SURGICAL, POLYMERIC |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03491 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | OTHER |
| Narrative | (B)(4). TO DATE, THE DEVICE HAS NOT BEEN RETURNED. IF THE PRODUCT IS RETURNED FOR EVALUATION, ANY FURTHER INFORMATION DERIVED FROM THE EVALUATION WILL BE SUBMITTED IN A SUPPLEMENTAL 3500A FORM. |
| Source | openFDA MAUDE (device adverse events) |
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