Model Number N/A |
Device Problem
Material Frayed (1262)
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Patient Problems
Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 05/04/2023 |
Event Type
malfunction
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Event Description
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It was reported by the customer "a colleague told me about the discovery of a non-externalized mandrel just before the connection of the catheter to the infusion, removed with difficulty in the absence of a "swollen" proximal end." no other information was provided.
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Manufacturer Narrative
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The date of event was not provided by the complainant/reporter, the date reflected in this report is the date bd became aware of the event.The device has not been returned to the manufacturer for evaluation.
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Manufacturer Narrative
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H11: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
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Event Description
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It was reported by the customer "a colleague told me about the discovery of a non-externalized mandrel just before the connection of the catheter to the infusion, removed with difficulty in the absence of a "swollen" proximal end." no other information was provided.
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Search Alerts/Recalls
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