VENTRALIGHT ST MESH Adverse Event — Injury (MDR 1213643-2020-04036)
VENTRALIGHT ST MESH Adverse Event — Injury (MDR 1213643-2020-04036) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VENTRALIGHT ST MESH; Generic name: SURGICAL MESH; Manufacturer: DAVOL INC., SUB. C.R. BARD, INC. -1213643.
| Device | VENTRALIGHT ST MESH |
|---|---|
| Generic name | SURGICAL MESH |
| Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. -1213643 |
| Report number | 1213643-2020-04036 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | Other, Consumer |
| Narrative | AT THIS TIME NO CONCLUSIONS CAN BE MADE. THE PATIENT'S ATTORNEY ALLEGES SURGICAL INTERVENTION AND "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 PROVIDED. NO LOT NUMBER HAS BEEN PROVIDED; THEREFORE, A REVIEW OF THE MANUFACTURING RECORDS IS NO |
| Source | openFDA MAUDE (device adverse events) |
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