80FRN HOSPIRA COSTA RICA LTD.

THE CUSTOMER INDICATED THE DEVICE WAS DISCARDED. (B) (4)

THE CUSTOMER CONTACT REPORTED A LEAK OF THERAPY CRITICAL FOR THIS PT. THE TUBING SET WAS BEING USED FOR DELIVERY OF AN UNSPECIFIED CONCENTRATION OF MILRINONE. NO SPECIFIC PUMP PARAMETERS WERE PROVIDED. IT WAS REPORTED THAT WHILE THE PT WAS SLEEPING, AN UNSPECIFIED VOLUME OF MEDICATION LEAKED FROM THE FILTER AIR VENT. THE CUSTOMER CONTACT STATED THE PT REPORTED LIGHT HEADEDNESS AND WEAKNESS. THE TUBING SET WAS REPLACED AND THE THERAPY WAS RESUMED. AFTER THE MILRINONE THERAPY WAS RESUMED, IT WAS REPORTED THE PT'S SYMPTOMS SUBSIDED. NO MEDICAL INTERVENTIONS WERE REQUIRED. ALTHOUGH THERE WAS POTENTIAL FOR SERIOUS INJURY, THERE WAS NO REPORTED CHANGE IN THE PT'S CLINICAL STATUS. INFO WAS REQUESTED FROM THE CUSTOMER CONTACT REGARDING DELIVERY RATE, PT'S VITAL SIGNS AND RECOVERY TIME. NO ADDITIONAL INFO WAS PROVIDED.

THE CUSTOMER CONTACT REPORTED A LEAK OF THERAPY CRITICAL FOR THIS PT. THE TUBING SET WAS BEING USED FOR DELIVERY OF AN UNSPECIFIED CONCENTRATION OF MILRINONE. NO SPECIFIC PUMP PARAMETERS WERE PROVIDED. IT WAS REPORTED THAT WHILE THE PT WAS SLEEPING, AN UNSPECIFIED VOLUME OF MEDICATION LEAKED FROM THE FILTER AIR VENT. THE CUSTOMER CONTACT STATED THE PT REPORTED LIGHT HEADEDNESS AND WEAKNESS. THE TUBING SET WAS REPLACED AND THE THERAPY WAS RESUMED. AFTER THE MILRINONE THERAPY WAS RESUMED, IT WAS REPORTED THE PT'S SYMPTOMS SUBSIDED. NO MEDICAL INTERVENTIONS WERE REQUIRED. ALTHOUGH THERE WAS POTENTIAL FOR SERIOUS INJURY, THERE WAS NO REPORTED CHANGE IN THE PT'S CLINICAL STATUS. INFO WAS REQUESTED FROM THE CUSTOMER CONTACT REGARDING DELIVERY RATE, PT'S VITAL SIGNS AND RECOVERY TIME. NO ADDITIONAL INFO WAS PROVIDED.

THE CUSTOMER INDICATED THE DEVICE WAS DISCARDED. (B) (4)

THE CUSTOMER CONTACT REPORTED A LEAK OF THERAPY CRITICAL FOR THIS PT. THE TUBING SET WAS BEING USED FOR DELIVERY OF AN UNSPECIFIED CONCENTRATION OF MILRINONE. NO SPECIFIC PUMP PARAMETERS WERE PROVIDED. IT WAS REPORTED THAT WHILE THE PT WAS SLEEPING, AN UNSPECIFIED VOLUME OF MEDICATION LEAKED FROM THE FILTER AIR VENT. THE CUSTOMER CONTACT STATED THE PT REPORTED LIGHT HEADEDNESS AND WEAKNESS. THE TUBING SET WAS REPLACED AND THE THERAPY WAS RESUMED. AFTER THE MILRINONE THERAPY WAS RESUMED, IT WAS REPORTED THE PT'S SYMPTOMS SUBSIDED. NO MEDICAL INTERVENTIONS WERE REQUIRED. ALTHOUGH THERE WAS POTENTIAL FOR SERIOUS INJURY, THERE WAS NO REPORTED CHANGE IN THE PT'S CLINICAL STATUS. INFO WAS REQUESTED FROM THE CUSTOMER CONTACT REGARDING DELIVERY RATE, PT'S VITAL SIGNS AND RECOVERY TIME. NO ADDITIONAL INFO WAS PROVIDED.

THE CUSTOMER INDICATED THE DEVICE WAS DISCARDED. (B) (4)

THE CUSTOMER INDICATED THE DEVICE WAS DISCARDED. (B) (4)

THE CUSTOMER CONTACT REPORTED A DISCONNECTION. THE TUBING SET WAS BEING USED FOR AN EPIDURAL DELIVERY OF AN UNSPECIFIED MEDICATION. AT AN UNSPECIFIED TIME, THE TUBING DISCONNECTED AT AN UNSPECIFIED LOCATION. THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS AND NO REPORTED DELAY OF THERAPY CRITICAL TO THIS PATIENT. NO MEDICAL INTERVENTIONS WERE REQUIRED. INFORMATION WAS REQUESTED FROM THE CUSTOMER REGARDING THE LOCATION OF THE DISCONNECTION, WHEN AND HOW THE DISCONNECTION WAS NOTED AND IF THE TUBING SET WAS REPLACED OR RECONNECTED; HOWEVER, NO ADDITIONAL INFORMATION WAS PROVIDED.