Catalog Number 320-10-00 |
Device Problem
Insufficient Information (3190)
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Patient Problems
Pain (1994); Ambulation Difficulties (2544)
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Event Date 10/28/2014 |
Event Type
malfunction
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Event Description
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Revision due to pain and limited mobility.This event report was received through clinical data collection activities.
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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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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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Revision due to pain and limited mobility.Original surgery date: (b)(6) 2011.Surgeon believes the event is unlikely related to the device or procedure.This event report was received through clinical data collection activities.
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Search Alerts/Recalls
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