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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It was reported a patient from home came in with blood underneath the access pack dressing, dressing removed to assess origin of blood, catheter with blood return and flushing well.It was stated a leak was noted to pack needle at the junction on needle tubing and hub.No detectable harm, just monitoring.
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