Catalog Number AK-05502 |
Device Problem
Break (1069)
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Patient Problem
Not Applicable (3189)
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Event Date 01/03/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has not been returned for investigation.Teleflex will continue to monitor and trend related events.
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Event Description
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The epidural tray contained broken vials.There was no injury.
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Manufacturer Narrative
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(b)(4).A lot number was not provided.A device history record review was performed based upon a lot number from sales history data.A device history record review was performed with a potentially relevant finding.A nonconformance was initiated to address broken ampule issues for lot# 23f18k0782.A lot number was not provided.A device history record review was performed based upon a lot number from sales history data.A device history record review was performed with a potentially relevant finding.A nonconformance was initiated to address broken ampule issues for lot# 23f18k0782.
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Event Description
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The epidural tray contained broken vials.There was no injury.
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Search Alerts/Recalls
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