C.R. BARD, INC. (BASD) -3006260740 BD DIALYSIS/HD CATHETER; CATHETER, HEMODIALYSIS, DUAL LUMEN, NON-IMPLANTED
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Model Number N/A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Erythema (1840); Swelling/ Edema (4577)
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Event Date 03/24/2021 |
Event Type
Injury
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Event Description
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It was reported during clinical assessment redness or swelling was identified at or around the central line insertion site.The events involved 1 dl dialysis neck,.
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Manufacturer Narrative
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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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Search Alerts/Recalls
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