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Catalog Number 140-36-93 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Joint Dislocation (2374)
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Event Date 06/01/2012 |
Event Type
malfunction
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Manufacturer Narrative
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The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation.Additionally, the device specific information was not provided, precluding a review of the device history record.
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Event Description
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Index surgery: (b)(6) 2012.On (b)(6), patient crossed legs and developed acute right hip pain.Surgeon performed closed reduction.On (b)(6), patient dislocated when getting up from a table.On (b)(6), patient dislocated again and surgeon performed closed reduction.This event report was received through clinical data collection activities.
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Search Alerts/Recalls
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