| Catalog Number |
115-378 |
| 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 |
11/11/2025
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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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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.
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Event or Problem Description
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Healthcare professional reported rupture and "textured".This record is for the right side.Device remains implanted.The device will be returned upon explantation.
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Additional Manufacturer Narrative
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Additional, changed, and/or corrected data: b5, d6b, h6.
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Event or Problem Description
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The device has been explanted.
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Additional Manufacturer Narrative
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Device evaluation: per the investigation procedure, the device is analyzed through visual inspection microscopic inspection if openings are observed and a weight verification.Per the analysis performed, the assessments of the complaints and any potential manufacturing issue are displayed along with any further actions required: ¿ rupture: observed broken device through microscopic inspection assessed as unidentified (tear) opening.No further actions are required as it is not related to the manufacturing process.¿ anxiety - product/ procedure: unable to observe through visual inspection as it is a physiological phenomenon.No additional observations performed on the device.No further actions are required.
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Event or Problem Description
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Healthcare professional reported rupture and "textured".This record is for the right side.The device has been explanted.
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Search Alerts/Recalls
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