C.R. BARD, INC. (BASD) -3006260740 BARD POWERMIDLINE CATHETER BASIC KIT (4F) (SINGLE-LUMEN) (20CM)
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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 02/22/2024 |
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.
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Event Description
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It was reported that nurse found the protective dressing contained a large amount of infusion fluid at the midline insertion site, lack of reflux after 2 days.The grip lock bandage was soaked.Ide redid the dressing, injected saline into the catheter and observed no leakage.2 hours after reconnecting the patient with his continuous iv treatment, a new liquid was stagnating under the dressing, still at the insertion site.No other information was provided.
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Manufacturer Narrative
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Initial medwatch report was submitted, upon further review it was found that this medwatch report 3006260740-2024-01070 is a duplicate file and has been voided.The original event was submitted on medwatch report 3006260740-2024-01120.
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Event Description
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It was reported that nurse found the protective dressing contained a large amount of infusion fluid at the midline insertion site, lack of reflux after 2 days.The grip lock bandage was soaked.Ide redid the dressing, injected saline into the catheter and observed no leakage.2 hours after reconnecting the patient with his continuous iv treatment, a new liquid was stagnating under the dressing, still at the insertion site.No other information was provided.
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