Catalog Number 5593240 |
Device Problems
Material Frayed (1262); Defective Component (2292)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 08/19/2023 |
Event Type
malfunction
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Event Description
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Customer reports that continuous renal replacement therapy treatment was performed on the patient's quasi-puncture femoral vein hemofiltration catheter.During the puncture, the guide wire was broken and a new dialysis catheter was used.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.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 device has not been returned to the manufacturer for evaluation.H3 other text : device not returned for evaluation.
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Event Description
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Customer reports that continuous renal replacement therapy treatment was performed on the patient's quasi-puncture femoral vein hemofiltration catheter.During the puncture, the guide wire was broken and a new dialysis catheter was used.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.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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Search Alerts/Recalls
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