Model Number 1050044 |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 01/27/2020 |
Event Type
Injury
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Manufacturer Narrative
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Pma/510k: reported device not marketed in the u.S., however, similar devices or devices that share components, raw materials, process methods or other technological characteristics are registered within the u.S.K111959.If additional information becomes available a follow up report will be submitted.
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Event Description
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It was reported that the ampoule leakage occurred.The reporter indicated when opening the package, the leakage from the ampule was already caused, therefore the product was not able to be used.
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Manufacturer Narrative
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Samples received: (b)(4) open pouch.Analysis and results: there is a previous complaint of this code-batch.We manufactured and distributed in the market (b)(4) units of this code-batch.There are no units in stock in b.Braun surgical's warehouse.We have received one open pouch that contains an unopened ampoule.The ampoule has been optically evaluated and a defect in the sealing bar of the ampoule (yellow bar at the bottom of the ampoule) was found.The leakage of the glue occurs at this point.We have conducted a review of the batch manufacturing record of this product and no deviations related to this issue have been found.Final conclusion: taking into account that the results of the sample received do not fulfil b.Braun surgical specifications, we conclude that the complaint is confirmed by evidence of failure in the sample received.Actions on distributed product of this reference/batch: based on the conclusion derived from investigation, it is not required to make actions in distributed product.Corrective/preventive actions: according to our internal procedures, we have opened a capa.
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Search Alerts/Recalls
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