USSC POLYSORB 3/0 Adverse Event — Malfunction (MDR 1219930-1997-01351)
USSC POLYSORB 3/0 Adverse Event — Malfunction (MDR 1219930-1997-01351) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: USSC POLYSORB 3/0; Generic name: BRAIDED SYNTHETIC ABSORBABLE SUTURE; Manufacturer: UNITED STATES SURGICAL CORP..
| Device | USSC POLYSORB 3/0 |
|---|---|
| Generic name | BRAIDED SYNTHETIC ABSORBABLE SUTURE |
| Manufacturer | UNITED STATES SURGICAL CORP. |
| Report number | 1219930-1997-01351 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 1997-06-20 |
| Report source | Foreign, Health Professional, User facility, Company representation |
| Narrative | 8/18/97-SUPPLEMENTAL REPORT #1 SUBMITTED TO FDA. DEVICE EVALUATION INDICATED AND CODES ENTERED IN H3 AND H6. |
| Source | openFDA MAUDE (device adverse events) |
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