VENTRALEX ST Adverse Event — Injury (MDR 1213643-2020-04102)
VENTRALEX ST Adverse Event — Injury (MDR 1213643-2020-04102) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VENTRALEX ST; Generic name: SURGICAL MESH; Manufacturer: DAVOL INC., SUB. C.R. BARD, INC. -1213643.
| Device | VENTRALEX ST |
|---|---|
| Generic name | SURGICAL MESH |
| Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. -1213643 |
| Report number | 1213643-2020-04102 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | Other, Consumer |
| Narrative | ATTORNEY ALLEGES THAT THE PATIENT UNDERWENT SURGERY FOR IMPLANT OF AN UNSPECIFIED BARD/DAVOL VENTRALEX ST ON (B)(6) 2012. AS REPORTED, THE PATIENT IS MAKING A CLAIM FOR AN ADVERSE PATIENT OUTCOME AGAINST THE VENTRALEX ST. ATTORNEY ALLEGES GENERAL ALLEGATIONS FOR "PAST, PRESENT, AND FUTURE DAMAGES, INCLUDING BUT NOT LIMITED TO, MENTAL AND PHYSICAL PAIN AND SUFFERING FOR SEVERE AND PERMANENT PERSONA |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →