C.R. BARD, INC. (BASD) -3006260740 BD PROVENA MIDLINE; CATHETER,INTRAVASCULAR,THERAPEUTIC,SHORT-TERM LESS THAN 30 DAYS
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Model Number N/A |
Device Problem
Failure to Infuse (2340)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 11/07/2022 |
Event Type
malfunction
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Manufacturer Narrative
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The information provided by bd represents all of the known information at this time.This complaint was received as part of a clinical survey.The customer filling in the survey opted to remain anonymous.Contact information and specific patient details were not disclosed as part of the survey.As such, additional information and the subject sample cannot be obtained.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.A lot history review (lhr) review is not possible, as no manufacturing lot number has been provided by the complainant.
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Event Description
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It was reported unable to use the guidewire to facilitate the placement of the midline catheter due to clotting.The event involves a 3fr provena midline it the basilic vein.
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Search Alerts/Recalls
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