TAYLOR SPATIAL FRAME 71070125

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2009-07-07 for TAYLOR SPATIAL FRAME 71070125 manufactured by Brooks Mfg Site.

Event Text Entries

[20624640] It was reported that during consolidation of the frame after distraction osteogenesis the ring broke at the connection point between the two half rings on the proximal ring of a tibial frame.
Patient Sequence No: 1, Text Type: D, B5


[20824993] Na
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1020279-2009-00608
MDR Report Key1412445
Report Source07
Date Received2009-07-07
Date of Report2009-07-06
Date Mfgr Received2009-06-25
Device Manufacturer Date2008-08-01
Date Added to Maude2009-07-15
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 Location0
Manufacturer ContactMR. JERRY HOWARD
Manufacturer Street1450 BROOKS RD.
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal38116
Manufacturer Phone9013996153
Manufacturer G1BROOKS MFG SITE
Manufacturer Street1450 BROOKS RD.
Manufacturer CityMEMPHIS TN 38116
Manufacturer CountryUS
Manufacturer Postal Code38116
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTAYLOR SPATIAL FRAME
Generic NameEXTERNAL FIXATOR / LYT
Product CodeLYT
Date Received2009-07-07
Returned To Mfg2009-07-06
Catalog Number71070125
Lot Number08HM01669
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBROOKS MFG SITE
Manufacturer AddressMEMPHIS TN US


Patients

Patient NumberTreatmentOutcomeDate
10 2009-07-07

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