DEKNATEL DEK BL MF 0 TC-43 2N 48" 833-123

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07,08 report with the FDA on 2011-09-08 for DEKNATEL DEK BL MF 0 TC-43 2N 48" 833-123 manufactured by Teleflex Medical.

Event Text Entries

[2237366] The event is reported as: complaint alleged: doctor used the capio - fired 6 times - it was working fine. The capio bullet got caught through the outside cage and when trying to release it he pulled the bullet needle off the suture. This happened outside the patient. The bullet needle got caught in the cage and could not be retrieved. Opened up another capio handle and procedure was finished without further complications. No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


[9414174] No sample is available for the manufacturer to evaluate. A follow-up report will be sent when investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004365956-2011-00365
MDR Report Key2269413
Report Source01,05,06,07,08
Date Received2011-09-08
Date of Report2011-08-30
Date of Event2011-08-29
Date Mfgr Received2011-08-30
Device Manufacturer Date2010-06-01
Date Added to Maude2012-04-26
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 FDA0
Event Location0
Manufacturer ContactJASMINE BROWN
Manufacturer StreetPO BOX 12600
Manufacturer CityDURHAM NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone9193614124
Manufacturer G1TELEFLEX
Manufacturer StreetAVE. TRANSFORMACION 5954 PARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO, TAMAULIPAS 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDEKNATEL DEK BL MF 0 TC-43 2N 48"
Generic NameCAPIO SUTURE
Product CodeMFJ
Date Received2011-09-08
Catalog Number833-123
Lot Number02F1003349
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressNUEVO LAREDO, TAMAULIPAS MX


Patients

Patient NumberTreatmentOutcomeDate
10 2011-09-08

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