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 with the FDA on 2017-04-03 for DEK BL MF 0 TC-43/HR 26 2N 36" 833-124 manufactured by Teleflex Medical.

Event Text Entries

[71838777] (b)(4). The device history record of batch number 74h1600336 has been reviewed and no issues or discrepancies were found which could potentially relate to this complaint. No rejection report was originated for the lot in question that can be associated to the complaint reported. The device history review shows that the product was assembled and inspected according to the manufacturing specifications. The facility has communicated that the device is not available for evaluation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[71838778] The bullet-tip came off in the patient during use. It was not retrieved. The patient's condition is unknown at this time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004365956-2017-00114
MDR Report Key6455189
Date Received2017-04-03
Date of Report2017-03-20
Date of Event2017-03-20
Date Mfgr Received2017-03-20
Device Manufacturer Date2016-08-02
Date Added to Maude2017-04-03
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE 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 Report0

Device Details

Brand NameDEK BL MF 0 TC-43/HR 26 2N 36"
Product CodeMFJ
Date Received2017-04-03
Catalog Number833-124
Lot Number74H1600336
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 2017-04-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.