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.A lot history review (lhr) review is not possible, as no manufacturing lot number has been provided by the complainant.
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It was reported "patient developed thrombophlebitis, approximately 15cm phlebitic zone along the basilic vein.Initial midline was occluded, no return flow, a second midline was installed, this time in the cephalic vein.Patient has had outpatient treatment for the thrombophlebitis.Doppler identified the 15cm thrombophlebitis on (b)(6) 2022.".
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