AHTB ACTIVE HEEL TRACTION BOOT 72202682

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-03-04 for AHTB ACTIVE HEEL TRACTION BOOT 72202682 manufactured by Smith & Nephew, Inc..

Event Text Entries

[187757074] (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[187757075] It was reported that, during a procedure, the active heel traction boot's strap broke while putting traction on the patient. It is unknown how the procedure was completed. A delay greater than 2 hours was reported. No patient injury was 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 Number3003604053-2020-00008
MDR Report Key9787979
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-03-04
Date of Report2020-03-04
Date of Event2020-02-10
Date Mfgr Received2020-02-10
Date Added to Maude2020-03-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 Street150 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAHTB ACTIVE HEEL TRACTION BOOT
Generic NameAPPARATUS, TRACTION, NON-POWERED
Product CodeHST
Date Received2020-03-04
Catalog Number72202682
OperatorHEALTH PROFESSIONAL
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 2020-03-04

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