BARD FLAT MESH Adverse Event — Injury (MDR 1213643-2020-04150)
BARD FLAT MESH Adverse Event — Injury (MDR 1213643-2020-04150) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BARD FLAT MESH; Generic name: SURGICAL MESH; Manufacturer: DAVOL INC., SUB. C.R. BARD, INC..
| Device | BARD FLAT MESH |
|---|---|
| Generic name | SURGICAL MESH |
| Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. |
| Report number | 1213643-2020-04150 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | ATTORNEY ALLEGES THAT ON OR ABOUT (B)(6) 1997, THE PATIENT UNDERWENT EPIGASTRIC HERNIA REPAIR. TWO BARD/DAVOL 3X6" MARLEX MESHES (BARD FLAT MESH), WERE IMPLANTED DURING THIS REPAIR. IT IS ALLEGED BY THE PATIENT'S ATTORNEY THAT ON OR ABOUT (B)(6) 2009, THE PATIENT UNDERWENT REVISION SURGERY TO THE BARD MESHES (BARD FLAT MESH). IT IS ALLEGED THAT ON OR ABOUT (B)(6) 2011, THE PATIENT WAS IMPLANTED WI |
| Source | openFDA MAUDE (device adverse events) |
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