Catalog Number 151650505 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Not Applicable (3189)
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Event Date 08/15/2018 |
Event Type
Injury
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Manufacturer Narrative
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Product complaint # (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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Event Description
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Patient with a attune knee implanted was complaining of knee pain and had a revision knee surgery performed.Patient consequence? :yes.Patient consequence description: knee pain.Action taken for procedure:replaced the attune knee with sigma revision implants.Is the information being submitted for this complaint all the details that are.Known/available regarding this event? : yes.
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Manufacturer Narrative
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Pc-(b)(4).No device associated with this report was received for examination.Depuy synthes considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.\ 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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Search Alerts/Recalls
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