VCL CT BRD UD 18IN 4-0 S/A P-3 PRM MP Adverse Event — Malfunction (MDR 2210968-2020-03526)
VCL CT BRD UD 18IN 4-0 S/A P-3 PRM MP Adverse Event — Malfunction (MDR 2210968-2020-03526) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VCL CT BRD UD 18IN 4-0 S/A P-3 PRM MP; Generic name: SUTURE, ABSORBABLE, SYNTHETIC; Manufacturer: ETHICON INC..
| Device | VCL CT BRD UD 18IN 4-0 S/A P-3 PRM MP |
|---|---|
| Generic name | SUTURE, ABSORBABLE, SYNTHETIC |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03526 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | (B)(4). A MANUFACTURING RECORD EVALUATION WAS PERFORMED FOR THE FINISHED DEVICE LOT PJU136, AND NO NON-CONFORMANCES WERE IDENTIFIED. ATTEMPTS HAVE BEEN MADE TO RETRIEVE THE DEVICE. TO DATE THE DEVICE HAS NOT BEEN RETURNED. IF THE DEVICE OR FURTHER DETAILS ARE RECEIVED AT A LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT. |
| Source | openFDA MAUDE (device adverse events) |
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