TRE-43 TRITON TABLE 7731

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-09-11 for TRE-43 TRITON TABLE 7731 manufactured by Chattanooga Group, Inc.

Event Text Entries

[3112838] Physical therapist was performing a grade v (thrust) mobilization to the pt's thoracic spine when the leaf of the treatment table supporting the pt's head and shoulders broke loose causing the pt and therapist to slide down table bumping the wall. Pt complained of increased neck and shoulder pain.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5026897
MDR Report Key2747013
Date Received2012-09-11
Date of Report2012-09-11
Date of Event2012-08-29
Date Added to Maude2012-09-17
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameTRE-43 TRITON TABLE
Generic NameTREATMENT TABLE
Product CodeINQ
Date Received2012-09-11
Catalog Number7731
Lot Number1450
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerCHATTANOOGA GROUP, INC
Manufacturer Address4717 ADAMS RD EIXSON TN 37343 US 37343


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2012-09-11

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