PORTEX? MINI-TRACH? II - NON SELDINGER KIT 100/461/000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-04-04 for PORTEX? MINI-TRACH? II - NON SELDINGER KIT 100/461/000 manufactured by Smiths Medical, Asd, Inc..

Event Text Entries

[104476606] (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[104476607] It was reported that after indwelling a tuohy needle in a patient, the customer attempted to insert the guidewire into it; but couldn't with the use of a portex? Mini-trach? Ii - non seldinger kit. No patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2018-00663
MDR Report Key7396086
Date Received2018-04-04
Date of Report2018-11-26
Date of Event2018-03-01
Date Mfgr Received2018-08-09
Device Manufacturer Date2017-07-28
Date Added to Maude2018-04-04
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 ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833310
Manufacturer G1SMITHS MEDICAL INTERNATIONAL LTD.
Manufacturer Street52 GRAYSHILL ROAD
Manufacturer CityCUMBERNAULD, GLASGOW G68 9HQ
Manufacturer CountryUK
Manufacturer Postal CodeG68 9HQ
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePORTEX? MINI-TRACH? II - NON SELDINGER KIT
Generic NameCRICOTHYROTOMY KIT
Product CodeOGP
Date Received2018-04-04
Returned To Mfg2018-04-24
Catalog Number100/461/000
Lot Number3457249
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL, ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
10 2018-04-04

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