TORQUE WRENCH 277040510

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-12-05 for TORQUE WRENCH 277040510 manufactured by Depuy Spine Inc.

Event Text Entries

[169274309] Reporter is a depuy employee. The device was received, the investigation is in progress, no conclusion could be drawn at the time of filing this report. Device was used for treatment, not diagnosis. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[169274310] It was reported that on an unknown date, during routine incoming inspection of a loaner set, it was observed that the torque handle was found to be out of drawing specification. There was no patient involvement. This complaint involves one (1) device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1526439-2019-52582
MDR Report Key9416620
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-12-05
Date of Report2019-11-13
Date Mfgr Received2019-12-30
Device Manufacturer Date2017-02-03
Date Added to Maude2019-12-05
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 ContactKARA DITTY-BOVARD
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone6103142063
Manufacturer G1BRIDGEWATER DISTRIBUTION
Manufacturer Street50 SCOTLAND BOULEVARD
Manufacturer CityBRIDGEWATER MA 02324
Manufacturer CountryUS
Manufacturer Postal Code02324
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTORQUE WRENCH
Generic NameWRENCH
Product CodeHXC
Date Received2019-12-05
Model Number277040510
Catalog Number277040510
Lot NumberKM839482
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY SPINE INC
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-05

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