ACTIVE HEEL TRACTION BOOT 72202682

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-07 for ACTIVE HEEL TRACTION BOOT 72202682 manufactured by Smith & Nephew, Inc..

Event Text Entries

[138289922] (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[138289923] It was reported that during hip arthroscopy, the boot plastic frame cracked. The procedure was successfully completed using a back-up device. A delay between 30 and 60 minutes was reported. No patient injury or other complications were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003604053-2019-00028
MDR Report Key8401264
Date Received2019-03-07
Date of Report2019-06-24
Date of Event2019-02-25
Date Mfgr Received2019-06-21
Date Added to Maude2019-03-07
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 ContactJIM GONZALES
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123585706
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street150 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameACTIVE HEEL TRACTION BOOT
Generic NameAPPARATUS, TRACTION, NON-POWERED
Product CodeHST
Date Received2019-03-07
Catalog Number72202682
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address150 MINUTEMAN ROAD ANDOVER MA 01810 US 01810


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-07

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