DEK BL MF 0 TC-43/HR 26 2N 36" 833-124

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 2015-08-25 for DEK BL MF 0 TC-43/HR 26 2N 36" 833-124 manufactured by Teleflex Medical.

Event Text Entries

[24000505] Qn#(b)(4). The device history review could not be conducted since the lot number was not provided. The device sample has not been returned to the manufacturer for investigation at the time of this report. The manufacturer will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[24000506] Alleged event: the harpoon broke and was left inside the patient. To insert the suture, a capio was used. A new capio and a new suture was used. At the second attempt the harpoon needle probably got stuck in capio. The harpoon needle was not found and a thread stuck out of the capio. The patient's condition was reported as unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004365956-2015-00223
MDR Report Key5029239
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2015-08-25
Date of Report2015-07-28
Date of Event2015-07-22
Date Mfgr Received2015-07-28
Date Added to Maude2015-08-25
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDEK BL MF 0 TC-43/HR 26 2N 36"
Generic NameSUTURE
Product CodeOVN
Date Received2015-08-25
Catalog Number833-124
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2015-08-25

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