| Catalog Number |
5531G211 |
| Medical Device Problem Code |
Insufficient Device Problem Information (3190)
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| Health Effect - Clinical Codes |
Unspecified Infection (1930); Injury (2348)
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| Date of Event |
08/25/2017
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Type of Reportable Event
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Serious Injury
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Additional Manufacturer Narrative
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Review of the device history records indicate that devices were manufactured and accepted into final stock with no relevant reported discrepancies.There have been no other events for the lot referenced.It was noted that the device is not available for evaluation.If additional information is received, it will be provided in a supplemental report upon completion of the investigation.The following devices were also listed in this report: triathlon cr fem comp #3 l-cem; cat#5510f301, lot#bxr7y.Triathlon prim cem fxd bplt #2; cat#5520b200; lot#can7t.Triathlon asymmetric x3 patella; cat#5551-g-299; lot#6jv6.It cannot be determined which, if any of these devices may have caused or contributed to the patient's experience.
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Event or Problem Description
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Procedure: patient underwent irrigation and debridement for pji with exchange of poly liner only.
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Event or Problem Description
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Procedure: patient underwent irrigation and debridement for pji with exchange of poly liner only.
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Additional Manufacturer Narrative
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An event regarding infection involving a triathlon insert was reported.The event was not confirmed.Method & results: device evaluation and results: not performed as the device was not returned for evaluation.Medical records received and evaluation: not performed as no medical records were provided.Device history review: indicated all devices were manufactured and accepted into final stock with no reported discrepancies.Complaint history review: there have been no other similar events for the reported lot or sterile lot referenced.Conclusions: the exact cause of the event could not be determined because insufficient information was provided.Further information such as medical records, operative reports and pathology reports including the strain of infection identified are needed to complete the investigation for determining a root cause.No further investigation is required at this time.If additional information becomes available to indicate further evaluation is warranted, this record will be reopened.
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Search Alerts/Recalls
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