During a visit with the hospital facility, a quest medical representative was informed of some issues with a few fluid delivery products.This report stated that when syringes are attached to the fluid delivery device and the set-up is bumped during a procedure, the ports have detached.The alleged event occurred during the induction of anesthesia.The report stated the clinician used other ports to administer the medicals of propofol, zemuron and fentanyl.There were no patient complication reported as a result of the alleged issue.The lot number of the device was not noted by the hospital.Any sample(s) were disposed of by the hospital and not given to the manufacturer for analysis.
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