inforMED
MalfunctionDRR

CARDIO LAB

Received Mar 31, 2005 · Event occurred Mar 22, 2005

Report MW1035079 · MDR key 588442

Device

Generic name

Electrophysiology Lab

Manufacturer

General Electric

Model number

CARDIO LAB II PLUS

Catalog number

*

Lot number

*

Product problems

  • False Reading From Device Non-Compliance

Patient

81 YR

  • Unknown (for use when the patient's condition is not known)

Narrative

Description of Event or Problem

PT HAD DECREASED BP - ART LINE INSERTED FOR CONTINUOUS PRESSURE MONITORING. TRANSDUCER ZEROED; NIBP CORRECTED WITH ARTERIAL PRESSURE. UNABLE TO MONITOR NIBP ARTERIAL PRESSURE CONTINUOUSLY DUE TO LIMITATION OF SYSTEM, SO ARTERIAL PRESSURE MONITORED E. LOGGED. NIBP CORRELATED WITH ARTERIAL PRESSURE PRIOR TO ARTERIAL SHEATH REMOVAL. WHEN SHEATH REMOVED, TRANSDUCER DISCONNECTED FORM PRESSURE CABLE - MATHEMATICALLY CORRECT NUMBER DISPLAYED UNDER PRESSURE (I.E. 127/60/83). NUMBERS CONT'D TO CHANGE AS IF PRESSURE WAS STILL BEING MONITORED. PRESSURE CABLE DISCONNECTED FROM AMPLIFIER - SYSTEM CONT'D TO DISPLAY PRESSURE NUMBERS. QUESTIONING RELIABILITY OF INVASIVE PRESSURE MONITORING - TREATING AN INACCURATE PRESSURE COULD LEAD TO PT HARM. THIS IS A RECURRENT PROBLEM THAT HAD BEEN ADDRESSED WITH GE IN NOV. '04.

Description of Event or Problem

ADD'L INFO REC'D FROM MFR 1/13/06: THE OPERATION REPORTED BY THE CUSTOMER IS ACCORDING TO DESIGN SPECIFICATIONS AND PRODUCT LABELING. THE CUSTOMER REPORTED THE INVASIVE BLOOD PRESSURE CABLE WAS DISCONNECTED FROM THE AMPLIFIER INPUT, INDICATING THE CUSTOMER AWARENESS OF THIS ACTION. THE CUSTOMER FURTHER REPORTED THAT THE OBSERVED VALUES IN THE BLOOD PRESSURE PARAMETER WINDOW WERE CONFUSING. THE MAC-LAB AND CARDIOLAB SYSTEM OPERATORS MANUALS CAUTION USERS TO NOT DISPLAY CHANNELS WHICH HAVE UNUSED CATHETER INPUT MODULES. TESTING VERIFIED THE REPORTED COMPLAINT. THE OPERATORS MANUALS CAUTION USERS ABOUT AND PROVIDE INSTRUCTIONS ON HOW TO AVOID.