Model Number N/A |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/01/2023 |
Event Type
malfunction
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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.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.H3 other text : device not received.
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Event Description
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It was reported by the customer that the following was obtained during clinical assessment: fluid leaking from central line insertion site.No other information was provided.
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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.This complaint was received as part of a clinical survey.Contact information was requested but not provided by the customer in the survey process.As such, any additional information including regarding the patient or subject sample cannot be obtained.
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Event Description
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It was reported by the customer that the following was obtained during clinical assessment: fluid leaking from central line insertion site.18g placed in the upper arm.No other information was provided.
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Search Alerts/Recalls
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