UNKNOWN TRIDENT X3 32ID LATERALLY OFFSET LINER Adverse Event — Injury (MDR 0002249697-2020-00811)
UNKNOWN TRIDENT X3 32ID LATERALLY OFFSET LINER Adverse Event — Injury (MDR 0002249697-2020-00811) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN TRIDENT X3 32ID LATERALLY OFFSET LINER; Generic name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC; Manufactu
| Device | UNKNOWN TRIDENT X3 32ID LATERALLY OFFSET LINER |
|---|---|
| Generic name | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC |
| Manufacturer | STRYKER ORTHOPAEDICS-MAHWAH |
| Report number | 0002249697-2020-00811 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | REPORTED EVENT: AN EVENT REGARDING DISLOCATION INVOLVING UNKNOWN TRIDENT X3 32ID LATERALLY OFFSET LINER WAS REPORTED. THE EVENT WAS NOT CONFIRMED. METHOD & RESULTS: DEVICE EVALUATION AND RESULTS: NOT PERFORMED AS PRODUCT WAS NOT RETURNED. CLINICIAN REVIEW: NO MEDICAL RECORDS WERE RECEIVED FOR REVIEW WITH A CLINICAL CONSULTANT DEVICE HISTORY REVIEW: COULD NOT BE PERFORMED AS LOT CODE INFORMATION WA |
| Source | openFDA MAUDE (device adverse events) |
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