Catalog Number UNK_SEL |
Device Problems
Device Dislodged or Dislocated (2923); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Failure of Implant (1924); Injury (2348)
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Event Date 11/01/2001 |
Event Type
Injury
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Manufacturer Narrative
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This complaint has been reported during a literature review performed by the post market surveillance group.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.The reported device was manufactured and distributed by small bone innovation, inc., (b)(4) and implanted before stryker became the legal manufacturer.On april 1, 2015 stryker became the legal manufacturer of the star system and has taken the responsibility for the medical device reporting.Device disposition is unknown.
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Event Description
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The manufacturer became aware of a literature from st.Michael¿s hospital, canada.The title of this report is ¿intermediate to long-term outcomes of total ankle replacement with the scandinavian total ankle replacement (star)¿ which is associated with the stryker ¿scandinavian total ankle replacement (star)¿ system.Within that publication, post-operative complications/ adverse events were reported, which occurred from november 2001 to october 2005.It was not possible to ascertain specific device details from the report, a review of the complaint handling database, however, revealed that the events have not been reported by the hospital or by the author of the publication, therefore 64 complaints were initiated retrospectively for adverse events mentioned in the report.This product inquiry addresses talar component subsidence followed by revision.The report states: ¿thirteen (12%) of the ankles required metal component revision.Seven of the ankles were converted to tibiotalocalcaneal arthrodesis¿.
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Event Description
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The manufacturer became aware of a literature from (b)(6) canada.The title of this report is ¿intermediate to long-term outcomes of total ankle replacement with the scandinavian total ankle replacement (star)¿ which is associated with the stryker ¿scandinavian total ankle replacement (star)¿ system.Within that publication, post-operative complications/ adverse events were reported, which occurred from (b)(6)2001 to (b)(6) 2005.It was not possible to ascertain specific device details from the report, a review of the complaint handling database, however, revealed that the events have not been reported by the hospital or by the author of the publication, therefore 64 complaints were initiated retrospectively for adverse events mentioned in the report.This product inquiry addresses talar component subsidence followed by revision.The report states: ¿thirteen (12%) of the ankles required metal component revision [¿] [¿] seven of the ankles were converted to tibiotalocalcaneal arthrodesis¿.
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Manufacturer Narrative
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New information in section h6 (device code and patient code).
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Search Alerts/Recalls
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