DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG 382800

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-04-03 for DURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG 382800 manufactured by Teleflex Medical.

Event Text Entries

[104421248] (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


[104421250] It was reported that the elastic seems to be brittle and/or breaking. There was no reported patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003898360-2018-00237
MDR Report Key7391874
Date Received2018-04-03
Date of Report2018-03-27
Date of Event2018-03-27
Date Mfgr Received2018-05-11
Device Manufacturer Date2017-06-13
Date Added to Maude2018-04-03
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 ContactJASMINE BROWN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9193614124
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetRANCHO EL DESCANSO
Manufacturer CityTECATE 21478
Manufacturer CountryMX
Manufacturer Postal Code21478
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameDURAHOOK 1/4 HOOK 10 PKG/BX 6 HKS/PKG
Product CodeGDG
Date Received2018-04-03
Returned To Mfg2018-04-30
Catalog Number382800
Lot Number73F1700330
Device Expiration Date2018-11-19
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2018-04-03

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