SFX SYM PDS+ UNI VIO 18IN 1 S/A CT Adverse Event — Malfunction (MDR 2210968-2020-03520)
SFX SYM PDS+ UNI VIO 18IN 1 S/A CT Adverse Event — Malfunction (MDR 2210968-2020-03520) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SFX SYM PDS+ UNI VIO 18IN 1 S/A CT; Generic name: SUTURE, SURGICAL, ABSORBABLE; Manufacturer: ETHICON INC..
| Device | SFX SYM PDS+ UNI VIO 18IN 1 S/A CT |
|---|---|
| Generic name | SUTURE, SURGICAL, ABSORBABLE |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03520 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | (B)(4). DATE SENT TO THE FDA: 06/08/2020. ADDITIONAL INFORMATION WAS REQUESTED AND THE FOLLOWING WAS OBTAINED: NO PATIENT CONSEQUENCE HAPPENED. |
| Source | openFDA MAUDE (device adverse events) |
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