Catalog Number 230787002 |
Device Problem
Device Difficult to Setup or Prepare (1487)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 11/06/2017 |
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 devices in question could not be locked when connected each other before delivery to the customer on (b)(6) 2017.It was brand new and the first use when the issue occurred.There was no surgical delay and no harm to the patient.
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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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Product complaint # pc-(b)(4).Investigation summary functional evaluation of the returned device was unable to replicate 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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Search Alerts/Recalls
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