TRIDENT CERAMIC LINER Adverse Event — Injury (MDR 9616680-2008-00030)
TRIDENT CERAMIC LINER Adverse Event — Injury (MDR 9616680-2008-00030) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRIDENT CERAMIC LINER; Generic name: IMPLANT; Manufacturer: STRYKER ORTHOPAEDICS CORK.
| Device | TRIDENT CERAMIC LINER |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER ORTHOPAEDICS CORK |
| Report number | 9616680-2008-00030 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Foreign, Distributor |
| Narrative | THE DISTRIBUTOR REPORTED ON BEHALF OF THE SURGEON, THAT THE TRIDENT CERAMIC LINER CRACKED. IT IS FURTHER REPORTED THAT FOLLOWING AN ARTICLE IN THE CORK EXAMINER NEWSPAPER AND INFORMATION ON THE FDA WEBSITE, THE PATIENT WAS REVISED. |
| Source | openFDA MAUDE (device adverse events) |
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