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 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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Facility reported to the sales rep, "product kinks a lot easier than the powerpicc sv, they are aware of the kinking at the insertion site if you don¿t make a large enough loop.They feel they have seen kinking more so in the vessel as the picc crosses over into the auxiliary vein, primary when they insert the picc into vessels that might have a unique path to the auxiliary such as many bifurcations".No patient injury was reported.
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