Model Number 1365-52-000 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Joint Laxity (4526); Physical Asymmetry (4573)
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Event Date 03/02/2022 |
Event Type
Injury
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Event Description
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Patient complained of hip pain follow tha.Upon reviewing films, doctor felt patient had some poly wear and required replacement.A dual mobility was implanted for greater stability and leg length.Doi: (b)(6) 2009, dor: (b)(6) 2022, affected side: right hip affected.
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Manufacturer Narrative
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(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.
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Search Alerts/Recalls
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