Catalog Number 121722052 |
Device Problems
Loss of Osseointegration (2408); Osseointegration Problem (3003); Appropriate Term/Code Not Available (3191)
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Patient Problems
Foreign Body Reaction (1868); Inflammation (1932); Pain (1994); Joint Swelling (2356); Limited Mobility Of The Implanted Joint (2671); No Code Available (3191)
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Event Date 09/09/2014 |
Event Type
Injury
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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.This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.
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Event Description
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Patient was revised to address elevated metal ion levels (cobalt=73.5, chromium=0.2), and metalosis.Update (b)(6) 2016 - pfs and medical records received.Pfs and medical records reviewed for mdr reportability.Pfs reported pain, limited mobility, swelling and metallosis.Revision surgical report noted metallosis, staining, and early cup loosening with abundant gray fluid, complete staining of synovium, acetabular posterior bone had begun to erode and metal stained tissue and bone behind cup.Pathology report noted chronic inflammation.Part/lot updated and cup added for loosening.
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Manufacturer Narrative
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No device associated with this report was received for examination.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.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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Udi: (b)(4).
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Event Description
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Ppf alleges metal wear.
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Manufacturer Narrative
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Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.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.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot : null.Device history batch : null.Device history review : null.If information is obtained that was not available for the initial medwatch, a follow-up medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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