The information provided by bard 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 bard.The device has not been returned to the manufacturer, at this time, for evaluation.A lot history review (lhr) review is not possible, as no manufacturing lot number has been provided by the complainant.Device not yet returned for evaluation.
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It was reported by the facility, via the sales rep, that the line was reportedly assessed to be leaking under the dressing.Upon examination of the line under the dressing, a tear was noted at the 12 cm mark.Securacath was present and the line measured at 15 cm external and 20 cm internal.No patient harm was reported.
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