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, at this time, for evaluation.A lot history review (lhr) of reby2218 showed one other similar product complaints from this lot number.
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It was reported that the healthcare professional was having difficulty accessing the patient and attempted to de-access the patient.When attempting to remove the device the needle came out, but the wire and the catheter remained in the patient.Patient was sent to interventional radiology, they were unable to remove the device and the vascular surgeon was called.
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