ENCORE MEDICAL L.P HEAD, FEMORAL, CERAMIC, BILOX DELTA, 28MM NEUTRAL; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTED OR NON-POROUS
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Catalog Number 400-03-282 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Joint Laxity (4526)
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Event Date 04/02/2024 |
Event Type
Injury
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Event Description
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Revision surgery - due to loosening.
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Manufacturer Narrative
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Complaint has been evaluated and is similar to previous report number 1644408-2021-01283; 400-04-360, s810 - device loosening, revision surgery.If additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.
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Search Alerts/Recalls
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