OFFSET SWIVAL CLAMP BAR & TRAPEZE, HEAVY DUTY 00-0640-021

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 2008-12-12 for OFFSET SWIVAL CLAMP BAR & TRAPEZE, HEAVY DUTY 00-0640-021 manufactured by Zimmer Orthopaedic Surgical Products.

Event Text Entries

[1034096] Clamps broke during use.
Patient Sequence No: 1, Text Type: D, B5


[8162797] Additional catalog #: 00-0640-003.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1035617-2008-00015
MDR Report Key1310024
Report Source05
Date Received2008-12-12
Date of Report2008-11-14
Date of Event2008-11-10
Date Mfgr Received2008-11-14
Date Added to Maude2010-04-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactJOHN WATKINS
Manufacturer Street200 WEST OHIO AVENUE
Manufacturer CityDOVER OH 44622
Manufacturer CountryUS
Manufacturer Postal44622
Manufacturer Phone3303649483
Manufacturer G1ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS
Manufacturer Street2021 OLD MOUNTAIN ROAD
Manufacturer CitySTATESVILLE NC 28677
Manufacturer CountryUS
Manufacturer Postal Code28677
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOFFSET SWIVAL CLAMP BAR & TRAPEZE, HEAVY DUTY
Generic NameCLAMP BAR & TRAPEZE
Product CodeILZ
Date Received2008-12-12
Catalog Number00-0640-021
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER ORTHOPAEDIC SURGICAL PRODUCTS
Manufacturer AddressSTATESVILLE NC US


Patients

Patient NumberTreatmentOutcomeDate
10 2008-12-12

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