Catalog Number 350-10-03 |
Device Problems
Fracture (1260); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Bone Fracture(s) (1870); Joint Disorder (2373); No Code Available (3191)
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Event Date 06/07/2017 |
Event Type
Injury
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Manufacturer Narrative
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The contribution of the device to the experience reported could not be determined as the device was not returned for evaluation.
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Event Description
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Patient experienced a medial malleolar fracture and had a reoperation to place a plate on the medial side.
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Event Description
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Patient experienced a right medial malleolar fracture.This is one of four products involved with the reported event and the associated manufacturer report numbers are 1038671-2017-00417, 1038671-2017-00419 and 1038671-2017-00420.
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Manufacturer Narrative
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This device is used for treatment not diagnosis.
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Search Alerts/Recalls
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