| Catalog Number |
68LP-325 |
| Medical Device Problem Code |
Fluid/Blood Leak (1250)
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| Health Effect - Clinical Code |
Failure of Implant (1924)
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| Date of Event |
08/22/2025
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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 "deflation" confirmed via ultrasound.This record is for the right side.Device has been explanted.
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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.Trend summary confirmed: the review of historical complaints on the complaint management handling indicates that there were no other records related to this event for units manufactured on lot number 3674831.The search criteria for these queries are mentioned in qpp07-01-004-her1-g02 rev: 7.0.The review of all potential trend evaluations for breast implants closed during the past 12 months indicates that no confirmed complaint trends have been observed for the event a050401 fluid/blood leak.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: deflation.
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Additional Manufacturer Narrative
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Additional, changed, and/or corrected data: d9, h3, h6.Device evaluation: based on the product analysis performed, the assessments of the complaint codes are: ¿ deflation: observed an opening assessed as surgical damage.As per the investigation procedure, creases, and wear abrasion were observed and none of the observations are found to be potentially related to the manufacturing process, no further actions are required.
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Event or Problem Description
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Healthcare professional reported "deflation" confirmed via ultrasound.This record is for the right side.Device has been explanted.
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Search Alerts/Recalls
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