| Catalog Number |
468-230 |
| 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 |
01/27/2026
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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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Further information from the reporter regarding event, product, or patient details has been requested.No additional information is available at this time.A review of the device history record has been completed.No deviations or non-conformances noted.Reason for reoperation: deflation.
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Event or Problem Description
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Healthcare professional reported ¿deflation¿.This record is for the right side.Device remains implanted.
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Additional Manufacturer Narrative
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Additional, changed, and/or corrected data: b5, b6, d4, d6b, h6.
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Event or Problem Description
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Additionally reported was "any creases" and "hole, non-specific".The device has been explanted.
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Event or Problem Description
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Healthcare professional reported ¿deflation¿.Later healthcare professional reported ¿any creases¿.This record is for the right side.Device was explanted.
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Additional Manufacturer Narrative
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Additional, changed, and/or corrected data: b5, d9, h3, h6.Device evaluation:
per the analysis performed, the assessments of the complaints and any potential manufacturing issue are displayed along with any further actions required:
- deflation: observed two openings through microscopic inspection assessed as fold flaw opening and surgical damage.No further actions are required as it is not related to the manufacturing process.- crease / folding of implant: observed creases on device through visual inspection.No further actions are required as it is not related to the manufacturing process.No additional observations performed on the device.No further actions are required.
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Search Alerts/Recalls
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