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Model Number 395.126 |
Device Problem
Device-Device Incompatibility (2919)
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Patient Problem
No Patient Involvement (2645)
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Event Type
malfunction
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Manufacturer Narrative
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Additional code: ktt.Reporter is company representative.Investigation summary: product was not returned.Based on the information available, it has been determined that no corrective and preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device history: part/lot combination are unknown at synthes gmbh, no dhr review possible.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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Event Description
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Device report from synthes reports an event in (b)(6) as follows: it was reported during an inspection of the minifixer system, it is noted that the holding and connecting clamps do not function appropriately with the other devices.No patient involvement.This is report 5 of 10 for (b)(4).This complaint is linked to (b)(4) and (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.H10 additional narrative: h3, h6: the device has been received, the investigation is in progress, no conclusion could be drawn at the time of filing 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.H3, h6: a product investigation was conducted.Visual inspection: holding clamp ø1.6 f/mini-ext-fix (part# 395.126, lot# 1362940, qty# (b)(4) ) was returned and received at us cq.Upon visual inspection at cq, it is observed that the device shows some rust which would not contribute to the complaint condition.No other damages were noticed with the device.Functional testing: complete functional testing of the device received was not performed at cq as the mating devices were not returned at cq.But all the components of the device were disassembled and assembled as intended without any issues.Dimensional inspection: dimensional inspection of the connecting rod hole in the clamp was performed at cq.The diameter of the hole of the clamp was measured and is within specification as per the relevant drawing.Document/specification review: the relevant drawings were reviewed during the investigation.No design issues or discrepancies were noticed.Investigation conclusion: the complaint condition cannot be confirmed for the holding clamp ø1.6 f/mini-ext-fix (part# 395.126, lot# 1362940).While a definitive root cause for the reported problem cannot be determined, it is possible that improper maintenance might have contributed to rust formed on the device.There were no issues during the manufacture of this product that would contribute to this complaint condition.During the investigation, no product design issues, or discrepancies were observed that may have contributed to the complaint condition.Based upon these results, no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Therefore, it has been determined that no corrective and/or preventive action is proposed.H3, h4, h6: a device history record (dhr) review was conducted: part: 395.126, lot: 1362940, manufacturing site: hägendorf, release to warehouse date: 15 june 2005.A manufacturing record evaluation was performed for the finished device lot number, and no non-conformances were identified.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.If the information is unknown, not available or does not apply, the section/field of the form is left blank.H10: additional narrative: d10 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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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.H3, 4, h6: device history lot, part: 395.126, lot: 1362940, manufacturing site: hägendorf, release to warehouse date: 15 june 2005.A manufacturing record evaluation was performed for the finished device lot number, and no non-conformances were identified.Investigation summary: background: 04/06/2020: updated event description: performing a review of the falange minifixer system, it is evident that the system bars do not enter the patella properly.For now, the system is blocked for operation due to incomplete key pieces.395.133 * 2 units, 395.125 * 2 units, 395.126 * 1 units.This complaint involves twenty-three (23) devices.Investigation flow: functional.Visual inspection: holding clamp ø1.6 f/mini-ext-fix (part# 395.126, lot# 1362940, qty# 1) was returned and received at us cq.Upon visual inspection at cq, it is observed that the device shows some rust which would not contribute to the complaint condition.No other damages were noticed with the device.Functional testing: complete functional testing of the device received was not performed at cq as the mating devices were not returned at cq.But all the components of the device were disassembled and assembled as intended without any issues.Can the complaint be replicated with the returned device(s)? unable to perform.Dimensional inspection: (gauge pins: gp29/ gp32).Dimensional inspection of the connecting rod hole in the clamp was performed at cq.The diameter of the hole of the clamp was measured and is within specification.Document/specification review: the drawings were reviewed during the investigation: no design issues or discrepancies were noticed.Complaint was not confirmed.Investigation conclusion: the complaint condition cannot be confirmed for the holding clamp ø1.6 f/mini-ext-fix (part# 395.126, lot# 1362940).While a definitive root cause for the reported problem cannot be determined, it is possible that improper maintenance might have contributed to rust formed on the device.There were no issues during the manufacture of this product that would contribute to this complaint condition.During the investigation, no product design issues, or discrepancies were observed that may have contributed to the complaint condition.Based upon these results, no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Therefore, it has been determined that no corrective and/or preventive action is proposed.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.11.Corrected data.
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