MATRESPONDER TOURNIQUET

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 2019-04-23 for MATRESPONDER TOURNIQUET manufactured by Pyng Medical.

Event Text Entries

[142815091] (b)(4). The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[142815092] It was reported that while the paramedic was tightening the turn key the tourniquet snapped.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011137372-2019-00131
MDR Report Key8541686
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-23
Date of Report2019-02-17
Date of Event2019-02-17
Date Mfgr Received2019-06-04
Date Added to Maude2019-04-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJASMINE BROWN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9193614124
Manufacturer G1TELEFLEX MEDICAL
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal Code27560
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMATRESPONDER TOURNIQUET
Generic NameNONPNEUMATIC TOURNIQUET
Product CodeGAX
Date Received2019-04-23
Catalog NumberMATR
Lot Number12228
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerPYNG MEDICAL


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-23

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