| Model Number |
TRM-445 |
| Medical Device Problem Code |
Material Rupture (1546)
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| Health Effect - Clinical Code |
Failure of Implant (1924)
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| Date of Event |
03/22/2023
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Type of Reportable Event
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Serious Injury
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Event or Problem Description
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Healthcare professional reported left side rupture.Device has been explanted and replaced.
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Additional Manufacturer Narrative
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A review of the device history record has been completed.No deviations or non-conformances noted.Further information from the reporter regarding event, product, or patient details has been requested.No additional information is available at this time.Reason for reoperation: rupture.Visual analysis of the photographs identified: anxiety-product/procedure: unable to confirm as it is a medical event not related to the device.Rupture: observed an opening the device but cannot perform an assessment of the opening as no microscopic analysis can be performed.It is not possible to determine the lot number or catalog through the photos provided.
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Event or Problem Description
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Healthcare professional reported, left side rupture.And textured implant concern.Device has been explanted and replaced.
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Event or Problem Description
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Healthcare professional reported left side rupture and textured implant concern.Device has been explanted and replaced.
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Additional Manufacturer Narrative
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Device evaluation: based on the device analysis grid, the assessments of the complaint are: rupture: observed a broken sharp assessed as unidentified (tear) opening (shell thickness was within specification) and missing piece of the shell assessed as to inconclusive.Anxiety-product/procedure: unable to confirm as it is a medical event not related to the device.Additional observations: crease flat observed in the device.No further actions are required as the device was implanted.
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Search Alerts/Recalls
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