ENCORE MEDICAL L.P ALTIVATE REVERSE, HUMERAL STEM, STANDARD SHELL, SZ 12X108MM; PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
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Catalog Number 530-12-108 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Joint Dislocation (2374); Implant Pain (4561)
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Event Date 01/31/2024 |
Event Type
Injury
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Manufacturer Narrative
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Complaint has been evaluated and is similar to previous report number 1644408-2021-00116; 533-10-108, s807 - pain, s803 - dislocation, revision surgery.If additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.
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Event Description
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Revision surgery - due to dislocation and pain.
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Search Alerts/Recalls
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