Catalog Number UNK ATTUNE FEMORAL |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Pain (1994); Not Applicable (3189); No Code Available (3191)
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Event Date 12/03/2019 |
Event Type
Injury
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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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Event Description
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The patient was revised to address painful knee and suspected patella, femoral issue.Loosening not suspected.Implants were not loose- surgeon removed and replaced with components with a tc3 rp.Attune rapture of arthrotomy.Attune cemented cr.Doi: (b)(6) 2018; dor: (b)(6) 2019; right knee.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary = > the device associated with this report was not received for examination.Depuy synthes considers the investigation closed at this time.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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