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Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Insufficient Information (4580)
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Event Date 01/01/2024 |
Event Type
Injury
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Manufacturer Narrative
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Additional information, including the product investigation, will be submitted within 30 days of receipt.
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Event Description
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It was reported that a 69 yo male patient, initial right shoulder implanted on an unknown date, underwent a revision procedure on an unknown date.The surgeon converted the failed stemless anatomic shoulder to a reverse shoulder.He removed the stemless components and caged glenoid and implanted a competitor¿s reverse shoulder.There were no surgical delays or device breakages during the procedure.No x-rays were able to be obtained.The patient was last known to be in stable condition following the event.No device returns available, reason unknown.Device images were provided.No further information.
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Search Alerts/Recalls
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