MESHGRAFT II COMPLETE Adverse Event — Malfunction (MDR 0001526350-2020-00417)
MESHGRAFT II COMPLETE Adverse Event — Malfunction (MDR 0001526350-2020-00417) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MESHGRAFT II COMPLETE; Generic name: EXPANDER, SURGICAL, SKIN GRAFT; Manufacturer: ZIMMER SURGICAL, INC..
| Device | MESHGRAFT II COMPLETE |
|---|---|
| Generic name | EXPANDER, SURGICAL, SKIN GRAFT |
| Manufacturer | ZIMMER SURGICAL, INC. |
| Report number | 0001526350-2020-00417 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL, USER FACI |
| Narrative | THIS EVENT HAS BEEN RECORDED BY ZIMMER BIOMET UNDER (B)(4). ONCE AN INVESTIGATION OF THE DEVICE IS COMPLETED, A FOLLOW-UP/FINAL REPORT WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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