CADD ADMINISTRATION SET- NON FLOW STOP 21-7036-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-29 for CADD ADMINISTRATION SET- NON FLOW STOP 21-7036-01 manufactured by Smiths Medical Asd, Inc.

Event Text Entries

[185481457] Information was received indicating that the cadd administration set leaked at the filter during priming. There was no reported injury or adverse events.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02356
MDR Report Key9895097
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-29
Date of Report2020-03-29
Date of Event2020-02-25
Date Mfgr Received2020-02-28
Device Manufacturer Date2019-09-24
Date Added to Maude2020-03-29
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 CityMINNEAPLOIS, MN
Manufacturer CountryUS
Manufacturer Phone3833310
Manufacturer G1SMITHS MEDICAL ASD, INC
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCADD ADMINISTRATION SET- NON FLOW STOP
Generic NameSET, ADMINISTRATION, INTRAVASCULAR
Product CodeFPA
Date Received2020-03-29
Model Number21-7036-01
Catalog Number21-7036-01
Lot Number3873550
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-29

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