FEMORAL CR IMPACTOR PAD Adverse Event — Malfunction (MDR 0001822565-2020-01505)
FEMORAL CR IMPACTOR PAD Adverse Event — Malfunction (MDR 0001822565-2020-01505) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FEMORAL CR IMPACTOR PAD; Generic name: PROSTHESIS, KNEE; Manufacturer: ZIMMER BIOMET, INC..
| Device | FEMORAL CR IMPACTOR PAD |
|---|---|
| Generic name | PROSTHESIS, KNEE |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001822565-2020-01505 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | (B)(4). THE PRODUCT HAS BEEN RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. |
| Source | openFDA MAUDE (device adverse events) |
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