TRITON TREATMENT TABLE TRE-DH5

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-11-30 for TRITON TREATMENT TABLE TRE-DH5 manufactured by Chattanooga Group.

Event Text Entries

[20897192] When the plastic shaft of the hand switch which holds the switch in position breaks, the switch stays in the on position. The switch broke while a pt was on the table. The pt was removed but the table had to be unplugged to stop it from going down. The table has been in use for two yrs; this was the second time the hand switch had broken.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1004220
MDR Report Key18059
Date Received1994-11-30
Date of Report1994-11-28
Date Added to Maude1994-12-01
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameTRITON TREATMENT TABLE
Product CodeINW
Date Received1994-11-30
Model NumberTRE-DH5
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key17987
ManufacturerCHATTANOOGA GROUP
Manufacturer AddressHIXSON TN 37342 US


Patients

Patient NumberTreatmentOutcomeDate
10 1994-11-30

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