SAUNDERS CERVICAL TRACTION 199594

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 2012-02-21 for SAUNDERS CERVICAL TRACTION 199594 manufactured by Djo, Llc.

Event Text Entries

[17558087] Lawsuit alleges, pt suffered back injury requiring medical intervention. It is unclear if the failure of the devices pump were related to the injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616086-2012-00012
MDR Report Key2467286
Report Source06
Date Received2012-02-21
Date of Report2012-02-22
Date of Event2010-01-18
Date Mfgr Received2012-01-23
Date Added to Maude2012-02-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer Street1430 DECISION ST.
Manufacturer CityVISTA CA 92081
Manufacturer CountryUS
Manufacturer Postal92081
Manufacturer Phone7607271280
Manufacturer G1EMPI, INC.
Manufacturer Street205 HWY 22 EAST
Manufacturer CityCLEAR WATER SD 57226
Manufacturer CountryUS
Manufacturer Postal Code57226
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSAUNDERS CERVICAL TRACTION
Generic NameTRACTION POWERED - TABLES & TRACTION
Product CodeIRS
Date Received2012-02-21
Model Number199594
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDJO, LLC
Manufacturer AddressVISTA CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2012-02-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.