Catalog Number 102408300 |
Device Problem
Insufficient Information (3190)
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Patient Problems
Pain (1994); No Code Available (3191)
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Event Date 12/08/2014 |
Event Type
Injury
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Event Description
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Patient was revised to address pain.
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Manufacturer Narrative
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This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.(b)(4).
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Manufacturer Narrative
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(b)(4).No device associated with this report was received for examination.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Based on previous investigations this complication of joint replacement is unlikely to have been the result of a device failing to meet required specifications.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Corrective action was not indicated.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.
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Manufacturer Narrative
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This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.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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Update rec'd 01/05/2015 - patient's medical records were received.Records were reviewed for mdr reportability.According to the medical records the patient was revised to address instability as well.There is no new information that would change the existing mdr decision.
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Search Alerts/Recalls
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