Catalog Number 690-00-22D |
Device Problems
Break (1069); Fracture (1260); Device Dislodged or Dislocated (2923); Material Integrity Problem (2978)
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Patient Problems
Injury (2348); Joint Dislocation (2374); No Information (3190)
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Event Date 06/11/2015 |
Event Type
Injury
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Event Description
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Constrained liner ring broke and patient dislocated.
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Manufacturer Narrative
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An evaluation of the device cannot be performed as the device was not returned due to hospital policy.Additional information has been requested and if received, will be provided in the supplemental report.Not returned to manufacturer.
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Manufacturer Narrative
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Review of the device history records indicates the lot was manufactured and accepted into final stock on 13-aug-2014.There have been no other events for the lot referenced.The event was confirmed by the provided x-rays.However, the root cause of the reported event coulc not be determined due to the minimal information received.No further investigation for this event is possible at this time as insufficient information was received by stryker orthopaedics.If additional information becomes available, this investigation will be reopened.
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Event Description
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Constrained liner ring broke and patient dislocated.
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Search Alerts/Recalls
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