Catalog Number 300-01-14 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Fall (1848); No Code Available (3191)
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Event Date 11/29/2018 |
Event Type
Injury
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Manufacturer Narrative
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Pending evaluation.
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Event Description
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Index surgery: (b)(6) 2018.Revision due to patient fall.
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Manufacturer Narrative
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Engineering evaluation noted that the revision reported was likely the result of nerve irritation due to the positioning and/or length of one of the compression screws used to secure the glenoid plate.
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Manufacturer Narrative
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Engineering evaluation noted that the revision reported was likely the result of the patient's fall, which led to loosening of the humeral stem and fracture of the greater and lesser tuberosities.
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Search Alerts/Recalls
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