TRAPEZE * 00-0640-067

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2005-09-12 for TRAPEZE * 00-0640-067 manufactured by Zimmer Orthopaedic Surgical Pr.

Event Text Entries

[417229] Pt pulled on trapeze. Bolt holding the "eye" to the "u" shaped coupler fell off and the trapeze fell, allegedly hitting the pt in the face.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1035617-2005-00006
MDR Report Key665348
Report Source05
Date Received2005-09-12
Date of Report2005-08-15
Date of Event2005-08-03
Date Facility Aware2005-08-03
Report Date2005-08-15
Date Reported to Mfgr2005-08-11
Date Mfgr Received2005-08-11
Date Added to Maude2006-01-20
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 FDA3
Event Location3
Manufacturer ContactJOY ELKINS
Manufacturer Street200 WEST OHIO AVENUE
Manufacturer CityDOVER OH 44622
Manufacturer CountryUS
Manufacturer Postal44622
Manufacturer Phone3303649483
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRAPEZE
Generic NameTRACTION ACCESSORY
Product CodeILZ
Date Received2005-09-12
Model Number*
Catalog Number00-0640-067
Lot Number*
ID Number*
OperatorOTHER
Device AvailabilityY
Device AgeNO INFO
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedI
Device Sequence No1
Device Event Key654755
ManufacturerZIMMER ORTHOPAEDIC SURGICAL PR
Manufacturer Address200 WEST OHIO AVENUE DOVER OH 44622 US
Baseline Brand NameTRAPEZE
Baseline Generic NameTRACTION ACCESSORY
Baseline Model No*
Baseline Catalog No00-0640-067
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-09-12

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