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 03/28/2019 |
Event Type
Injury
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Event Description
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It was reported that a revision surgery was performed due to of cup dislocation, shell, liner and head removed and replaced with depuy products.Stem left insitu.
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Manufacturer Narrative
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The associated complaint device was not returned.The medical investigation concluded that no clinically relevant supporting documentation was provided; therefore, a thorough medical investigation could not be performed.Should clinical documentation become available in the future, the clinical/medical task may be re-evaluated.No further medical assessment is warranted at this time.Without the actual product involved and/or device information, our investigation cannot proceed.If the device or new information is received in the future, the complaint can be re-opened.No further actions are being taken at this time.We consider this investigation closed.Credit cannot be issued for the device.
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Search Alerts/Recalls
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