Catalog Number 5513-001 |
Device Problem
Defective Component (2292)
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Patient Problem
No Patient Involvement (2645)
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Event Date 05/14/2019 |
Event Type
malfunction
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Manufacturer Narrative
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A review of the device history record has been initiated.If any deviations or non-conformance are found, a supplemental medwatch will be submitted.Serial number (b)(4), lot number 62812.Device labeling: precautions: the xen®45 gel stent and xen® injector should be carefully examined in the operating room prior to use.
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Event Description
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Healthcare professional reported needle was shorter than specification against the xen®45 gts.Surgery was completed with another xen.There was no eye injury.
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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.Device evaluation: the needle tip of the injector was measured against a certified ruler.The needle was measured at 3.5mm and were determined to be within the limits of the design specifications.The reported complaint of the xen glaucoma treatment system was not confirmed.The returned unit needle tip was measured to be 3.5mm.There were no other anomalies observed.The manufactured xen systems are 100% tested in-process and inspected at manufacturing.Allergan will continue to monitor the frequency of these complaints to determine if there is a trend or if this was an individual occurrence.
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Event Description
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Healthcare professional reported needle was shorter than specification against the xen®45 gts.Surgery was completed with another xen.There was no eye injury.
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Search Alerts/Recalls
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