SMITH & NEPHEW, INC. HIP IMPLANT; PROSTHESIS, HIP, HEMI-, TRUNNION-BEARING, FEMORAL, METAL/POLYACETAL
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Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
No Information (3190)
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Event Type
Injury
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Event Description
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It was reported that a possible revision surgery was performed.
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Event Description
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It was reported that the patient has suffered from pain since long time ago.A revision surgery was performed due to unknown reasons, no information about the devices was provided.
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Manufacturer Narrative
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The associated complaint device was not returned.A clinical evaluation was conducted and no relevant clinical medical information was provided to conduct a thorough medical assessment.Without the actual product involved and/or device information, our investigation cannot proceed.If the device or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.
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Search Alerts/Recalls
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