ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL Adverse Event — Injury (MDR 2210968-2020-03475)
ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL Adverse Event — Injury (MDR 2210968-2020-03475) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL; Generic name: MESH, SURGICAL; Manufacturer: ETHICON INC..
| Device | ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL |
|---|---|
| Generic name | MESH, SURGICAL |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03475 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | OTHER |
| Narrative | DATE SENT TO FDA: (B)(6) 2020. H6 PATIENT CODES: 3191 - BOWEL PERFORATION; 3189 - SURGICAL INTERVENTION. ADDITIONAL INFORMATION: A1, A2, A4, B7, D1, D2, D4, D7, E1. ADDITIONAL B5 NARRATIVE: IT WAS REPORTED THAT THE PATIENT EXPERIENCED RECURRENCE, PAIN, ADHESIONS, AND A BOWEL PERFORATION. IT WAS REPORTED THAT THE PATIENT UNDERWENT A MESH REMOVAL ON (B)(6) 2017. |
| Source | openFDA MAUDE (device adverse events) |
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