Catalog Number 254501040 |
Device Problem
Device Damaged by Another Device (2915)
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Patient Problem
No Information (3190)
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Event Date 03/15/2017 |
Event Type
malfunction
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Manufacturer Narrative
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This complaint is under investigation.Depuy will notify the fda of the results of the investigation once it has been completed.(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 is no longer possible to use a 1.27mm saw blade in the instrument´s saw blade slit.
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Manufacturer Narrative
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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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Evaluation of the returned device was unable to confirm the reported event.The device functions as intended.Depuy considers the investigation closed at this time.Should the 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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Search Alerts/Recalls
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