AXIS *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1999-03-10 for AXIS * manufactured by Oxford Instruments - Medical Systems Div..

Event Text Entries

[175035] Oxford instruments axis central system (obstetrics) fails to alarm during signal loss with hewlett packard fetal monitors. The system operates properly with oxford sonicaid fetal monitors. On 6/10/98 there was an incident where the oxford fetal monitoring network failed to produce a signal loss alarm. There was no pt injury. Oxford instruments was notified and the trace was downloaded for evaluation. Subsequent investigation by the biomedical engineering dept revealed that none of the hewlett-packard fetal monitors connected the network produced a signal loss alarm. The monitors were tested by simulating a fetal heart rate of approx 120 beats per min and then discontinuing the signal. The problem was reproducible in every test. The bradycardia alarms worked on the hewlett-packard fetal monitors and both alarms worked when the test was performed on the meridian 800 monitors. The tests were documented and faxed to oxford instruments. Initial explanations from oxford were inadequate. Oxford stated that the loss occurred because the 1 min continuous trace criteria was never met. After reevaluating the pt trace and staff protests oxford verbally acknowledged that the 1 min criteria was met and that there was a problem with the latest software upgrade. (the problem occurred soon after the software was upgraded). Oxford was notified periodically about the lack of resolution of the problem but no date was given for the problem to be corrected. On 2/26/99 another incident occurred at the hosp where a signal loss alarm was not produced. Fortunately there was no pt injury. The decision was made to disconnect all hewlett-packard fetal monitors from the network.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1015877
MDR Report Key213907
Date Received1999-03-10
Date of Report1999-03-04
Date of Event1999-02-26
Date Added to Maude1999-03-16
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameAXIS
Generic NameCENTRAL FETAL MONITORING SYSTEM
Product CodeKXN
Date Received1999-03-10
Model NumberAXIS
Catalog Number*
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key207515
ManufacturerOXFORD INSTRUMENTS - MEDICAL SYSTEMS DIV.
Manufacturer Address11526 53RD ST. N. CLEARWATER FL 346204825 US


Patients

Patient NumberTreatmentOutcomeDate
10 1999-03-10

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