CROSSFIRE 10 DEG INSERT Adverse Event — Injury (MDR 9616680-2008-00031)
CROSSFIRE 10 DEG INSERT Adverse Event — Injury (MDR 9616680-2008-00031) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CROSSFIRE 10 DEG INSERT; Generic name: IMPLANT; Manufacturer: STRYKER ORTHOPAEDICS CORK.
| Device | CROSSFIRE 10 DEG INSERT |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER ORTHOPAEDICS CORK |
| Report number | 9616680-2008-00031 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT: PATIENT WAS A CHRONIC DISLOCATOR. LINER EXCHANGED TO A CONSTRAINED LINER. NO DEVICE MALFUNCTION HAS BEEN REPORTED. |
| Source | openFDA MAUDE (device adverse events) |
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