ULTRAPRO MESH UNKNOWN PRODUCT Adverse Event — Injury (MDR 2210968-2020-03599)
ULTRAPRO MESH UNKNOWN PRODUCT Adverse Event — Injury (MDR 2210968-2020-03599) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ULTRAPRO MESH UNKNOWN PRODUCT; Generic name: MESH, SURGICAL, POLYMERIC; Manufacturer: ETHICON INC..
| Device | ULTRAPRO MESH UNKNOWN PRODUCT |
|---|---|
| Generic name | MESH, SURGICAL, POLYMERIC |
| Manufacturer | ETHICON INC. |
| Report number | 2210968-2020-03599 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL, L |
| Narrative | (B)(4). THIS REPORT IS RELATED TO A JOURNAL ARTICLE; THEREFORE, NO PRODUCT WILL BE RETURNED FOR ANALYSIS AND THE BATCH HISTORY RECORDS CANNOT BE REVIEWED AS THE LOT NUMBER HAS NOT BEEN PROVIDED. ATTEMPTS ARE BEING MADE TO CLARIFY THE FOLLOWING INFORMATION. TO DATE NO RESPONSE HAS BEEN PROVIDED. IF FURTHER DETAILS ARE RECEIVED AT A LATER DATE A SUPPLEMENTAL MEDWATCH WILL BE SENT. DOES THE SURGEON B |
| Source | openFDA MAUDE (device adverse events) |
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