SMITH & NEPHEW, INC. HIP IMPLANT; PROSTHESIS, HIP, HEMI-, TRUNNION-BEARING, FEMORAL, METAL/POLYACETAL
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Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problem
Injury (2348)
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Event Date 08/20/2019 |
Event Type
Injury
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Event Description
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It was reported that a revision surgery was performed due to dislocation.Cup and liner were revised.
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Manufacturer Narrative
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Additional narrative: the associated complaint devices were not returned.The medical investigation concluded that several attempts have been made to obtain clinical medical documents to no avail.Without supporting clinical/medical documents, a thorough investigation cannot be performed.Should information become available these complaints can be re-assessed.Without the actual product involved and/ or product information, our investigation cannot proceed.If the devices or new information is received in the future, these complaints can be re-opened.No further actions are being taken at this time.We consider this investigation closed.
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Search Alerts/Recalls
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