Catalog Number 950502055 |
Device Problem
Separation Problem (4043)
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Patient Problem
Not Applicable (3189)
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Event Date 09/20/2018 |
Event Type
malfunction
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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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When the surgeon attempted to remove the connected keel punch impactor and the keel punch, the keel section remained within the tibia.It was then removed by use of kocher forceps.Surgery time was extended for less than 1 minute.
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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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Manufacturer Narrative
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Product complaint(b)(4).Investigation summary no device was received for examination, therefore the reported event could not be confirmed.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will 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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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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Search Alerts/Recalls
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