WRIGHTS LANE SYNTHES USA PRODUCTS LLC 26MM COCR RADIAL HEAD STANDARD HEIGHT/13.5MM-STERILE; PROSTHESIS, ELBOW, HEMI-RADIAL , POLYMER
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Model Number 09.402.026S |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Osteolysis (2377)
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Event Date 01/01/2018 |
Event Type
Injury
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Manufacturer Narrative
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Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.(b)(4).Without a lot number the device history records review could not be completed.Product was not returned.A review of the device history records has been requested.Device was used for treatment, not diagnosis.
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Event Description
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It was reported that on (b)(6) 2018, the patient underwent a removal surgery.The patient required an additional surgery to remove the cobalt chromium radial head standard height due to osteolysis following the implantation of radial head replacement.It was unknown if there was a surgical delay.Procedure outcome and patient status are unknown.This complaint involves two (2) device.This report is 1 of 2 for (b)(4).
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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.The incorrect date was inadvertently utilized in initial medwatch report.The correct date is november 26, 2018. device was used for treatment, not diagnosis.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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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.Device was used for treatment, not diagnosis.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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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.Additional narrative: device is not expected to be returned for manufacturer review/investigation.Remedial action initiated, removal reporting #, correctional #.Corrected data: reporter occupation.Device was used for treatment, not diagnosis.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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