SMITHS MEDICAL LEVEL 1 HOTLINE LOW FLOW SYSTEMS CON-HL-90

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-18 for SMITHS MEDICAL LEVEL 1 HOTLINE LOW FLOW SYSTEMS CON-HL-90 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[183964437] One fluid warmer was returned for evaluation. Visual inspection of the device found it to be in fair physical condition. The device was filled with water and set up with temperature check. It was noted that device did function as intended after the micro switch was replaced. However, the micro switch was damaged and fails to alert when disposable or temp check become detached. The microswitch was damaged as a result of user interface.
Patient Sequence No: 1, Text Type: N, H10


[183964438] Information was received that a smiths medical level 1 hotline low flow system had microswitch issue. No adverse effects reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02054
MDR Report Key9849706
Report SourceUSER FACILITY
Date Received2020-03-18
Date of Report2020-03-18
Date Mfgr Received2020-02-17
Device Manufacturer Date2015-01-13
Date Added to Maude2020-03-18
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 N
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street3350 GRANADA AVENUE NORTH SUITE 100
Manufacturer CityOAKDALE, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMITHS MEDICAL LEVEL 1 HOTLINE LOW FLOW SYSTEMS
Generic NameWARMER, BLOOD, NON-ELECTROMAGNETIC RADIATION
Product CodeBSB
Date Received2020-03-18
Returned To Mfg2019-05-23
Catalog NumberCON-HL-90
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-18

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