Catalog Number J133S-MV-12-T |
Device Problem
Patient-Device Incompatibility (2682)
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Patient Problem
Foreign Body Reaction (1868)
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Event Type
Injury
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Manufacturer Narrative
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The event of exposure is a physiological complication and analysis of the device generally does not assist allergan in determining a probable cause for this event.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: exposure.
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Event Description
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Healthcare professional reported right side " te broke through the skin and exposed suddenly".The device has been explanted.
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Event Description
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Healthcare professional reported right side " te broke through the skin and exposed suddenly".The device has been explanted.
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Manufacturer Narrative
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A review of the device history record has been completed.No deviations or non-conformances noted.
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Search Alerts/Recalls
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