Catalog Number 962711000 |
Device Problems
Mechanical Problem (1384); Device Dislodged or Dislocated (2923)
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Patient Problems
Injury (2348); Joint Disorder (2373); Joint Dislocation (2374); No Code Available (3191)
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Event Date 01/01/2020 |
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.
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Event Description
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The primary surgery was performed about 10 years ago (the date was unknown) via tha with the head (p/n: 962711000), the stem (p/n: 961172000), the liner (p/n: 121887358) and the cup (p/n: 121780058, (b)(6) product).It was reported that on an unknown date, the dislocation of the head was occurred.The revision surgery was scheduled on (b)(6), 2020.The reason of the dislocation was unknown.No further information is available.
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Manufacturer Narrative
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Product complaint#: (b)(4).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.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary : the devices were returned for investigation.No product defects were noted.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Corrective action was not indicated.Device history lot : 2583596.Device history review : no anomalies found.
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Manufacturer Narrative
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Product complaint # = > pc-(b)(4).No code available (3191) used to capture no information available.Added: d11 and h6 device code corrected: h6 (patient code: joint dislocation is being retracted as there is no reported dislocation in the event).
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Manufacturer Narrative
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Product complaint # (b)(4).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. .
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary: the devices were returned for investigation.No product defects were noted.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Corrective action was not indicated.Addendum added 16-september-2020.Following receipt of additional photographs, the investigation was re-opened and the photographs transferred to depuy bioengineering for review, with notification received that: ¿these images do not alter the findings of the previous bioengineering report.¿ no changes were required to the previous investigation conclusions.Device history lot: 2583596.Device history review: no anomalies found.
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Search Alerts/Recalls
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