MESH ¿ VENTRALEX Adverse Event — Injury (MDR 1213643-2020-04041)
MESH ¿ VENTRALEX Adverse Event — Injury (MDR 1213643-2020-04041) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MESH ¿ VENTRALEX; Generic name: SURGICAL MESH; Manufacturer: DAVOL INC., SUB. C.R. BARD, INC..
| Device | MESH ¿ VENTRALEX |
|---|---|
| Generic name | SURGICAL MESH |
| Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. |
| Report number | 1213643-2020-04041 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER, OTHER |
| Narrative | AT THIS TIME NO CONCLUSIONS CAN BE MADE. THE PATIENT'S ATTORNEY ALLEGES INTESTINAL BLOCKAGE, RECURRENCE, INFLAMMATION, SUBSEQUENT SURGICAL INTERVENTION, SEVERE PAIN AND GENERAL ALLEGATIONS FOR PAST, PRESENT, AND FUTURE DAMAGES, INCLUDING BUT NOT LIMITED TO, MENTAL AND PHYSICAL PAIN AND SUFFERING FOR SEVERE AND PERMANENT PERSONAL INJURIES SUSTAINED BY THE PATIENT; HOWEVER, NO DETAILS HAVE BEEN PROV |
| Source | openFDA MAUDE (device adverse events) |
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