The reported event could not be confirmed, since the device was not returned for evaluation and no other additional information is available.More detailed information about the complaint event as well as the affected device must be available in order to determine the root cause of the complaint event.The device history record could not be reviewed because the affected lot number was not communicated.If any further information is provided, the investigation report will be updated.Device disposition is unknown.
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The manufacturer became aware of a literature published by (b)(6) hospital, in (b)(6).The title of this report is ¿the influence of fracture stability on early patient mortality and reoperation after pertrochanteric and intertrochanteric hip fractures¿ which is associated with the stryker ¿gamma3 nailing¿ system.The article can be found at https://doi.Org/10.1097/bot.0000000000000359.Within that publication, post-operative complications were reported, which allegedly occurred from january 2003 to june 2007.It was not possible to ascertain specific device details or patient information from the report, or to match the events reported with previously reported complaints.Therefore, new complaints were initiated in the system for the post-operative complications mentioned in the report.This product inquiry addresses (2) cases of loosening/screw cut out requiring reoperation.
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