PERFIX PLUG Adverse Event — Injury (MDR 1213643-2020-04054)
PERFIX PLUG Adverse Event — Injury (MDR 1213643-2020-04054) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PERFIX PLUG; Generic name: SURGICAL MESH; Manufacturer: DAVOL INC., SUB. C.R. BARD, INC..
| Device | PERFIX PLUG |
|---|---|
| Generic name | SURGICAL MESH |
| Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. |
| Report number | 1213643-2020-04054 |
| 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 THAT THE PATIENT HAD SUBSEQUENT SURGICAL INTERVENTION; HOWEVER, NO DETAILS HAVE BEEN PROVIDED. NO LOT NUMBER HAS BEEN PROVIDED; THEREFORE, A REVIEW OF THE MANUFACTURING RECORDS IS NOT POSSIBLE. THIS EMDR REPRESENTS THE BARD/DAVOL PERFIX PLUG (DEVICE #2). AN ADDITIONAL EMDR WAS SUBMITTED TO REPRESENT THE BARD MESH (BARD FLAT ME |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →