TWINFIX TI 5.0 ULTRABRAID 72200755

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-01-23 for TWINFIX TI 5.0 ULTRABRAID 72200755 manufactured by Smith & Nephew, Inc..

Event Text Entries

[176311964] Foreign zipcode (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[176311965] It was reported that during surgery, when the twinfix titanium 5. 0 ultrabraid was being passing, it broke inside the patient. All the pieces were removed with a nipper. The procedure was completed without delay using a back-up device. No patient injury or other complications were reported. All available information has been disclosed. If additional information should become available, a supplemental report will be submitted accordingly.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219602-2020-00127
MDR Report Key9623577
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-23
Date of Report2020-03-10
Date of Event2020-01-08
Date Mfgr Received2020-03-06
Device Manufacturer Date2017-05-01
Date Added to Maude2020-01-23
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 ContactHOLLY TOPPING
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123913905
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street130 FORBES BOULEVARD
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal Code02048
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTWINFIX TI 5.0 ULTRABRAID
Generic NameSTAPLE, FIXATION, BONE
Product CodeJDR
Date Received2020-01-23
Model Number72200755
Catalog Number72200755
Lot Number50661649
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address130 FORBES BOULEVARD MANSFIELD MA 02048 US 02048


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-23

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