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, as the device was discarded after the event occurred.A lot history review (lhr) review is not possible; as no manufacturing lot number has been provided.
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It was reported that contrast medium allegedly flowed back through the sub route of the powerloc.Reportedly, during ct imaging with the powerport mri isp and the powerloc, when infusing contrast medium into the main rout of the powerloc, the medium allegedly flowed back from the sub route.Reportedly, prior to infusion, the operator exchanged the cap attached to the sub route for a non-pressure injection cap, connected a syringe, confirmed blood backflow, and flushed the catheter.There was no reported patient injury.
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