SMITH & NEPHEW, INC. HIP IMPLANT; PROSTHESIS, HIP, HEMI-, TRUNNION-BEARING, FEMORAL, METAL/POLYACETAL
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Device Problem
Insufficient Information (3190)
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Patient Problem
Injury (2348)
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Event Date 01/23/2020 |
Event Type
Injury
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Event Description
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It was reported that a revision surgery was performed due to unknown reasons.There is no information regarding to the explanted devices.
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Manufacturer Narrative
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The information received by the manufacturer has been re-evaluated for mdr reporting.The information states that the procedure was not a revision of smith and nephew devices, therefore, it was determined that this case does not meet the threshold for reporting and is a non-reportable event.If further details are provided confirming the occurrence of a reportable event, our files will be updated accordingly and a further report submitted outlining both the event details and our investigations performed.
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Search Alerts/Recalls
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