Catalog Number 217863180 |
Device Problem
Loose or Intermittent Connection (1371)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 11/15/2017 |
Event Type
malfunction
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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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It was reported that the reamer was damaged and will not stay on adapter.It was also reported that the t handle connection was damaged due to reamer being rounded off at connection point.
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Manufacturer Narrative
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Product complaint # (b)(4).
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Manufacturer Narrative
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Product complaint: (b)(4).Investigation summary: functional testing of the returned device confirmed the reported event.Depuy considers the investigation closed at this time.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).
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Search Alerts/Recalls
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