UNKNOWN LINER Adverse Event — Injury (MDR 0002249697-2020-00802)
UNKNOWN LINER Adverse Event — Injury (MDR 0002249697-2020-00802) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN LINER; Generic name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CE; Manufacturer: STRYKER ORTHOPAEDICS-MAHWAH.
| Device | UNKNOWN LINER |
|---|---|
| Generic name | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CE |
| Manufacturer | STRYKER ORTHOPAEDICS-MAHWAH |
| Report number | 0002249697-2020-00802 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | IF ADDITIONAL INFORMATION IS RECEIVED, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION. DEVICE NOT RETURNED. |
| Source | openFDA MAUDE (device adverse events) |
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