PHYSIOMESH Adverse Event — Injury (MDR 2210968-2020-03536)
PHYSIOMESH Adverse Event — Injury (MDR 2210968-2020-03536) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PHYSIOMESH; Generic name: MESH, SURGICAL, POLYMERIC; Manufacturer: ETHICON INC..
| Device | PHYSIOMESH |
|---|---|
| Generic name | MESH, SURGICAL, POLYMERIC |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03536 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | OTHER |
| Narrative | DATE SENT TO FDA: 05/04/2020. A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA. |
| Source | openFDA MAUDE (device adverse events) |
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