The hospital reported that during preparation for a coronary artery bypass procedure, hst iii system (3.8mm) did not load and fell to the floor.A new device was opened and used for the case.Never used on patient.No patient harm reported, as there was no patient involvement.
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Trackwise #(b)(4).The lot #25159629 history record review was completed.There were no ncmrs, rework, or deviations documented for the reported lot number.Based on the dhr/lhr review results, it was determined that there is no relation between the batch manufacturing process and the reported failure.
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