C.R. BARD, INC. (BASD) -3006260740 POWERLOC MAX POWER-INJECTIBLE INFUSION SET 20G X 0.75IN; SET, ADMINISTRATION, INTRAVASCULAR
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Model Number N/A |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problem
Chemical Exposure (2570)
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Event Date 09/18/2023 |
Event Type
malfunction
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Event Description
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It was reported by customer that upon flushing the mediport and connecting patient to ns flush bag, patient reported feeling wetness on her skin.Mediport needle and tubing was assessed, and it was noted that the ns was leaking around the clave.Patient de-accessed and re-accessed with a new needle.Additional information received 02 october 2023: leaking involved a hazardous drug spill on the area and patient.There were no pieces broken off.
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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 received by the manufacturer for evaluation.H3 other text : device not returned.
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Search Alerts/Recalls
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