COMPAX 40E

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2008-12-30 for COMPAX 40E manufactured by Ge Medical Systems, Llc.

Event Text Entries

[1026440] It was reported that the table locks did not actuate when the technologist released the foot pedal due to power loss, causing the tabletop to unexpectedly move in both lateral and longitudinal directions without resistance (free float). There was no injury reported. This situation could contribute to an injury if a patient or operator were unaware of this condition while loading or unloading a patient. The ensuing instability could lead to a fall.
Patient Sequence No: 1, Text Type: D, B5


[8168482] The ge field engineer (fe) found a blown fuse in the table base that powers the table locks. The fe replaced the fuse and verified that the locks were performing according to specifications.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2126677-2008-00106
MDR Report Key1301364
Report Source06
Date Received2008-12-30
Date of Report2008-10-21
Date of Event2008-10-21
Date Mfgr Received2008-10-21
Date Added to Maude2009-05-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMARTHA KAMROW
Manufacturer Street3000 N GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal53188
Manufacturer Phone2623127196
Manufacturer G1GE MEDICAL SYSTEMS, LLC
Manufacturer Street3000 N GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI 53188
Manufacturer CountryUS
Manufacturer Postal Code53188
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOMPAX 40E
Product CodeIZZ
Date Received2008-12-30
ID NumberSYSID 706721CMCR2
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerGE MEDICAL SYSTEMS, LLC
Manufacturer Address3000 N GRANDVIEW BLVD. WAUKESHA WI 53188 US 53188


Patients

Patient NumberTreatmentOutcomeDate
10 2008-12-30

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